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A systematic clinical review of prenatally diagnosed tetrasomy 9p


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Dutly F, Balmer D, Baumer A, Binkert F, Schinzel A. Isochromosomes 12p and 9p: parental origin and possible mechanisms of formation. Eur J Hum Genet. 1998; 6(2): 140-144.10.1038/sj.ejhg.52001689781058DutlyFBalmerDBaumerABinkertFSchinzelAIsochromosomes 12p and 9p: parental origin and possible mechanisms of formationEur J Hum Genet1998621401449781058Open DOISearch in Google Scholar

Ghymers D, Hermann B, Distèche C, Frederic J. Partial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations. [French] Humangenetik. 1973; 20(3): 273-282.GhymersDHermannBDistècheCFredericJPartial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations[French] Humangenetik197320327328210.1007/BF003857404772080Search in Google Scholar

Schaefer GB, Domek DB, Morgan MA, Muneer RS, Johnson SF. Tetrasomy of the short arm of chromosome 9: Prenatal diagnosis and further delineation of the phenotype. Am J Med Genet. 1991; 15;38(4): 612-615.10.1002/ajmg.13203804222063906SchaeferGBDomekDBMorganMAMuneerRSJohnsonSFTetrasomy of the short arm of chromosome 9: Prenatal diagnosis and further delineation of the phenotypeAm J Med Genet1991153846126152063906Open DOISearch in Google Scholar

Chen CP, Wang LK, Chern SR, Wu PS, Chen YT, Kuo YL, et al. Mosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecular cytogenetic characterization, and literature review. Taiwan J Obstet Gynecol. 2014; 53(1): 79-85.10.1016/j.tjog.2013.12.00224767652ChenCPWangLKChernSRWuPSChenYTKuoYLet alMosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecular cytogenetic characterization, and literature reviewTaiwan J Obstet Gynecol2014531798524767652Open DOISearch in Google Scholar

El Khattabi L, Jaillard S, Andrieux J, Pasquier L, Perrin L, Capri Y, et al. Clinical and molecular delineation of tetrasomy 9p syndrome: Report of 12 new cases and literature review. Am J Med Genet A. 2015; 167(6): 1252-1261.10.1002/ajmg.a.3693225847481ElKhattabi LJaillardSAndrieuxJPasquierLPerrinLCapriYet alClinical and molecular delineation of tetrasomy 9p syndrome: Report of 12 new cases and literature reviewAm J Med Genet A201516761252126125847481Open DOISearch in Google Scholar

Frémond ML, Gitiaux C, Bonnet D, Guiddir T, Crow YJ, de Pontual L, et al. Mosaic tetrasomy 9p: A Mendelian condition associated with pediatriconset overlap myositis. Pediatrics. 2015; 136(2): e544-e547.FrémondMLGitiauxCBonnetDGuiddirTCrowYJdePontual Let alMosaic tetrasomy 9p: A Mendelian condition associated with pediatriconset overlap myositisPediatrics20151362e544e54710.1542/peds.2015-072426216333Search in Google Scholar

Lazebnik N, Cohen L. Prenatal diagnosis and findings of tetrasomy 9p. J Obstet Gynaecol Res. 2015; 41(7): 997-1002.2594409610.1111/jog.12706LazebnikNCohenLPrenatal diagnosis and findings of tetrasomy 9pJ Obstet Gynaecol Res2015417997100225944096Search in Google Scholar

Orye E, Verhaaren H, Van Egmond H, Devloo-Blancquaert A. Anew case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX,+i(9p) and a peculiar congenital heart defect. Clin Genet. 1975; 7(2): 134-143.OryeEVerhaarenHVanEgmond HDevloo-BlancquaertAAnew case of the trisomy 9P syndromeReport of a patient with unusual chromosome findings (46,XX/47,XX,+i(9p) and a peculiar congenital heart defect. Clin Genet19757213414310.1111/j.1399-0004.1975.tb00309.x1132161Search in Google Scholar

Rutten FJ, Scheres JM, Hustinx TW, ter Haar BG. A presumptive tetrasomy for the short arm of chromosome 9. Humangenetik. 1974; 25(3): 163-170.4141333RuttenFJScheresJMHustinxTWterHaar BGA presumptive tetrasomy for the short arm of chromosome 9Humangenetik197425316317010.1007/BF002814234141333Search in Google Scholar

Wisniewski L, Politis GD, Higgins JV. Partial tetrasomy 9 In a liveborn infant. Clin Genet. 1978; 14(3): 147-153.WisniewskiLPolitisGDHigginsJVPartial tetrasomy 9 In a liveborn infantClin Genet197814314715310.1111/j.1399-0004.1978.tb02120.x699353Search in Google Scholar

Cavalcanti DP, Ferrari I, de Almeida JC, de Pina Neto JM, de Oliverira JA. Tetrasomy 9p caused by idic (9) (pter----q13----pter). Am J Med Genet. 1987; 27(3): 497-503.363112510.1002/ajmg.1320270303CavalcantiDPFerrariIdeAlmeida JCdePina Neto JMdeOliverira JATetrasomy 9p caused by idic (9) (pter----q13----pter)Am J Med Genet1987273497503Search in Google Scholar

Cuoco C, Gimelli G, Pasquali F, Poloni L, Zuffardi O, Alicata P, et al. Duplication of the short arm of chromosome 9. Analysis of five cases. Hum Genet. 1982; 61(1): 3-7.CuocoCGimelliGPasqualiFPoloniLZuffardiOAlicataPet alDuplication of the short arm of chromosome 9Analysis of five cases. Hum Genet19826113710.1007/BF00291321Search in Google Scholar

Garcia-Cruz D, Vaca G, Ibarra B, Sanchez-Corona J, Ocampo-Campos R, Peregrina S, et al. Tetrasomy 9p: Clinical aspects and enzymatic gene dosage expression. Ann Genet. 1982; 25(4): 237-242.6985014Garcia-CruzDVacaGIbarraBSanchez-CoronaJOcampo-CamposRPeregrinaSet alTetrasomy 9p: Clinical aspects and enzymatic gene dosage expressionAnn Genet1982254237242Search in Google Scholar

Moedjono SJ, Crandall BF, Sparkes RS. Tetrasomy 9p: Confirmation by enzyme analysis. J Med Genet. 1980; 17(3): 227-230.740113510.1136/jmg.17.3.227MoedjonoSJCrandallBFSparkesRSTetrasomy 9p: Confirmation by enzyme analysisJ Med Genet1980173227230Search in Google Scholar

McDowall AA, Blunt S, Berry AC, Fensom AH. Prenatal diagnosis of a case of tetrasomy 9p. Prenat Diagn. 1989; 9(11): 809-811.10.1002/pd.19700911102616538McDowallAABluntSBerryACFensomAHPrenatal diagnosis of a case of tetrasomy 9pPrenat Diagn1989911809811Open DOISearch in Google Scholar

Abe T, Morita M, Kawai K, Misawa S, Takino T, Hashimoto H, et al. Partial tetrasomy 9(9pter to 9q2101) due to an extra iso-dicentric chromosome. Ann Genet. 1977; 20(2): 111-114.AbeTMoritaMKawaiKMisawaSTakinoTHashimotoHet alPartial tetrasomy 9(9pter to 9q2101) due to an extra iso-dicentric chromosomeAnn Genet1977202111114Search in Google Scholar

Peters J, Pehl C, Miller K, Sandlin CJ. Case report of mosaic partial tetrasomy 9 mimicking Klinefelter syndrome. Birth Defects Orig Artic Ser. 1982; 18(3B): 287-293.7139111PetersJPehlCMillerKSandlinCJCase report of mosaic partial tetrasomy 9 mimicking Klinefelter syndromeBirth Defects Orig Artic Ser1982183B287293Search in Google Scholar

Balestrazzi P, Croci G, Frassi C, Franchi F, Giovannelli G. Tetrasomy 9p confirmed by GALT. J Med Genet. 1983; 20(5): 396-399.664477310.1136/jmg.20.5.396BalestrazziPCrociGFrassiCFranchiFGiovannelliGTetrasomy 9p confirmed by GALTJ Med Genet1983205396399Search in Google Scholar

Shapiro SD, Hansen KL, Littlefield CA. Brief clinical report: Non-mosaic partial tetrasomy and partial trisomy 9. Am J Med Genet. 1985; 20(2): 271-276.10.1002/ajmg.13202002103976720ShapiroSDHansenKLLittlefieldCABrief clinical report: Non-mosaic partial tetrasomy and partial trisomy 9Am J Med Genet1985202271276Open DOISearch in Google Scholar

Calvieri F, Tozzi C, Benincori C, De Merulis MV, Bellussi A, Genuardi M, et al. Partial tetrasomy 9 in an infant with clinical and radiological evidence of multiple joint dislocations. Eur J Pediatr. 1988; 147(6): 645-648.10.1007/BF00442483CalvieriFTozziCBenincoriCDeMerulis MVBellussiAGenuardiMet alPartial tetrasomy 9 in an infant with clinical and radiological evidence of multiple joint dislocationsEur J Pediatr19881476645648Open DOISearch in Google Scholar

Andou R, Mimaki T, Ogihara T, Tamai H, Mino M. A case of tetrasomy 9p. Acta Paediatr Jpn. 1994; 36(6): 724-726.10.1111/j.1442-200X.1994.tb03280.x7532895AndouRMimakiTOgiharaTTamaiHMinoMA case of tetrasomy 9pActa Paediatr Jpn1994366724726Open DOISearch in Google Scholar

Eggermann T, Rossier E, Theurer-Mainka U, Backsch C, Klein-Vogler U, Enders H, et al. New case of mosaic tetrasomy 9p with additional neurometabolic findings. Am J Med Genet. 1998; 75(5): 530-533.948979910.1002/(SICI)1096-8628(19980217)75:5<530::AID-AJMG14>3.0.CO;2-LEggermannTRossierETheurer-MainkaUBackschCKlein-VoglerUEndersHet alNew case of mosaic tetrasomy 9p with additional neurometabolic findingsAm J Med Genet1998755530533Search in Google Scholar

Jalal SM, Kukolich MK, Garcia M, Benjamin TR, Day DW. Tetrasomy 9p: An emerging syndrome. Clin Genet. 1991; 39(1): 60-64.1997218JalalSMKukolichMKGarciaMBenjaminTRDayDWTetrasomy 9p: An emerging syndromeClin Genet1991391606410.1111/j.1399-0004.1991.tb02986.xSearch in Google Scholar

Leichtman LG, Zackowski JL, Storto PD, Newlin A. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: Case report and comparison with trisomy 9p. Am J Med Genet. 1996; 63(3): 434-437.10.1002/(SICI)1096-8628(19960614)63:3<434::AID-AJMG4>3.0.CO;2-RLeichtmanLGZackowskiJLStortoPDNewlinANon-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: Case report and comparison with trisomy 9pAm J Med Genet1996633434437Open DOISearch in Google Scholar

Grass FS, Parke JC Jr, Kirkman HN, Christensen V, Roddey OF, Wade RV, et al. Tetrasomy 9p: Tissue-limited idic(9p) in a child with mild manifestations and a normal CVS result. Report and review. Am J Med Genet. 1993; 47(6): 812-816.10.1002/ajmg.1320470603GrassFSParkeJC JrKirkmanHNChristensenVRoddeyOFWadeRVet alTetrasomy 9p: Tissue-limited idic(9p) in a child with mild manifestations and a normal CVS resultReport and review. Am J Med Genet1993476812816Open DOISearch in Google Scholar

Melaragno MI, Brunoni D, Patrício FR, Corbani M, Mustacchi Z, dos Santos Rde C, et al. A patient with tetrasomy 9p, Dandy-Walker cyst and Hirschsprung disease. Ann Genet. 1992; 35(2): 79-84.1524413MelaragnoMIBrunoniDPatrícioFRCorbaniMMustacchiZdosSantos Rde Cet alA patient with tetrasomy 9p, Dandy-Walker cyst and Hirschsprung diseaseAnn Genet19923527984Search in Google Scholar

Nakamura Y, Sato E, Sakai Κ, Sakuma S, Hashimoto Τ, Sindou S. Abnormal chromosome 9 in a neonate program. Report of three cases. Arch Pathol Lab Med. 1990; 114(2): 185-187.NakamuraYSatoESakaiΚSakumaSHashimotoΤSindouSAbnormal chromosome 9 in a neonate programReport of three cases. Arch Pathol Lab Med19901142185187Search in Google Scholar

Papenhausen P, Riscile G, Miller K, Miller K, Kouisseff B, Tedesco T. Tissue limited mosaicism in a patient with tetrasomy 9p. Am J Med Genet. 1990; 37(3): 388-91.10.1002/ajmg.1320370319PapenhausenPRiscileGMillerKMillerKKouisseffBTedescoTTissue limited mosaicism in a patient with tetrasomy 9pAm J Med Genet199037338891Open DOISearch in Google Scholar

Park JP, Rawnsley BE, Marin-Padilla M. Tetrasomy 9p syndrome. Ann Genet. 1995; 38(1): 54-56.7625761ParkJPRawnsleyBEMarin-PadillaMTetrasomy 9p syndromeAnn Genet19953815456Search in Google Scholar

Stumm M, Tönnies H, Mandon U, Götze A, Krebs P, Wieacker PF. Mosaic tetrasomy 9p in a girl with multiple congenital anomalies: Cytogenetic and molecular-cytogenetic studies. Eur J Pediatr. 1999; 158(7): 571-575.10.1007/s004310051149StummMTönniesHMandonUGötzeAKrebsPWieackerPFMosaic tetrasomy 9p in a girl with multiple congenital anomalies: Cytogenetic and molecular-cytogenetic studiesEur J Pediatr19991587571575Open DOISearch in Google Scholar

Tonk VS. Moving towards a syndrome: A review of 20 cases and a new case of non-mosaic tetrasomy 9p with long-term survival. Clin Genet. 1997; 52(1): 23-29.TonkVSMoving towards a syndrome: A review of 20 cases and a new case of non-mosaic tetrasomy 9p with long-term survivalClin Genet1997521232910.1111/j.1399-0004.1997.tb02510.xSearch in Google Scholar

Van Hove J, Kleczkowska A, De Bruyn M, De Bruyn M, Bekaert J, Fryns JP. Tetrasomy 9p: prenatal diagnosis and fetopathological findings in a second trimester male fetus. Ann Genet. 1994; 37(3): 139-142.VanHove JKleczkowskaADeBruyn MDeBruyn MBekaertJFrynsJPTetrasomy 9p: prenatal diagnosis and fetopathological findings in a second trimester male fetusAnn Genet1994373139142Search in Google Scholar

Cazorla Calleja MR, Verdú A, Félix V. Dandy-Walker malformation in an infant with tetrasomy 9p. Brain Dev. 2003; 25(3): 220-223.10.1016/S0387-7604(02)00211-5CazorlaCalleja MRVerdúAFélixVDandy-Walker malformation in an infant with tetrasomy 9pBrain Dev2003253220223Open DOISearch in Google Scholar

Chen CP, Chang TY, Chern SR, Lee CC, Town DD, Lee MS, et al. Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis. Prenat Diagn. 2007; 27(4): 383-385.1739355610.1002/pd.1678ChenCPChangTYChernSRLeeCCTownDDLeeMSet alPrenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesisPrenat Diagn2007274383385Search in Google Scholar

Coman D, Bacic S, Boys A, Sparrow DB, Dunwoodie SL, Savarirayan R, et al. Spondylocostal dysostosis in a pregnancy complicated by confined placentai mosaicism for tetrasomy 9p. Am J Med Genet A. 2008; 146A(15): 1972-1976.10.1002/ajmg.a.32299ComanDBacicSBoysASparrowDBDunwoodieSLSavarirayanRet alSpondylocostal dysostosis in a pregnancy complicated by confined placentai mosaicism for tetrasomy 9pAm J Med Genet A2008146A1519721976Open DOISearch in Google Scholar

de Azevedo Moreira LM, Freitas LM, Gusmão FA, Riegel M. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl. Birth Defects Res A Clin Mol Teratol. 2003; 67(12): 985-988.10.1002/bdra.10126deAzevedo Moreira LMFreitasLMGusmãoFARiegelM.New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girlBirth Defects Res A Clin Mol Teratol20036712985988Open DOISearch in Google Scholar

Deurloo KL, Cobben JM, Heins YM, de Ru M, Wijnaendts LC, van Vugt JM. Prenatal diagnosis of tetrasomy 9p in a 19-week-old fetus with Dandy-Walker malformation: A case report. Prenat Diagn. 2004; 24(10): 796-798.10.1002/pd.850DeurlooKLCobbenJMHeinsYMdeRu MWijnaendtsLCvanVugt JM.Prenatal diagnosis of tetrasomy 9p in a 19-week-old fetus with Dandy-Walker malformation: A case reportPrenat Diagn20042410796798Open DOISearch in Google Scholar

Dhandha S, Hogge WA, Surti U, McPherson Ε. Three cases of tetrasomy 9p. Am J Med Genet. 2002; 113(4): 375-380.10.1002/ajmg.b.1082612457411DhandhaSHoggeWASurtiUMcPhersonΕThree cases of tetrasomy 9pAm J Med Genet2002113437538012457411Open DOISearch in Google Scholar

di Vera Ε, Liberati Μ, Celentano C, Calabrese G, Guanciali-Franchi PE, Morizio E, et al. Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. J Assist Reprod Genet. 2008; 25(11-12): 577-580.10.1007/s10815-008-9257-7diVera ΕLiberatiΜCelentanoCCalabreseGGuanciali-FranchiPEMorizioEet alRhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancyJ Assist Reprod Genet20082511-12577580259376818953648Open DOISearch in Google Scholar

Hengstschläger Μ, Bettelheim D, Drahonsky R, Repa C, Deutinger J, Bernaschaek G. Prenatal diagnosis of tetrasomy 9p with Dandy-Walker malformation. Prenat Diagn. 2004; 24(8): 623-626.10.1002/pd.93315305350HengstschlägerΜBettelheimDDrahonskyRRepaCDeutingerJBernaschaekGPrenatal diagnosis of tetrasomy 9p with Dandy-Walker malformationPrenat Diagn200424862362615305350Open DOISearch in Google Scholar

Henriques-Coelho T, Oliva-Teles N, Fonseca-Silva ML, Tibboel D, Guimarães Η, Corriea-Pinto J. Congenital diaphragmatic hernia in a patient with tetrasomy 9p. J Pediatr Surg. 2005; 40(10): e29-e31.Henriques-CoelhoTOliva-TelesNFonseca-SilvaMLTibboelDGuimarãesΗCorriea-PintoJCongenital diaphragmatic hernia in a patient with tetrasomy 9pJ Pediatr Surg20054010e29e3110.1016/j.jpedsurg.2005.06.03216226972Search in Google Scholar

Lloveras E, Pérez C, Solé F, Zamora L, Lladonosa A, Espinet B, et al. Two cases of tetrasomy 9p syndrome with tissue limited mosaicism. Am J Med Genet A. 2004; 124A(4): 402-406.10.1002/ajmg.a.2044714735590LloverasEPérezCSoléFZamoraLLladonosaAEspinetBet alTwo cases of tetrasomy 9p syndrome with tissue limited mosaicismAm J Med Genet A2004124A440240614735590Open DOISearch in Google Scholar

McAuliffe F, Winsor EJ, Chitayat D. Tetrasomy 9p mosaicism associated with a normal phenotype. Fetal Diagn Ther. 2005; 20(3): 219-222.1582450210.1159/000083909McAuliffeFWinsorEJChitayatDTetrasomy 9p mosaicism associated with a normal phenotypeFetal Diagn Ther200520321922215824502Search in Google Scholar

Ogino W, Takeshima Y, Nishiyama A, Yagi M, Oka N, Matsuo M. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production. Kobe J Med Sci. 2007; 53(4): 143-50.17932453OginoWTakeshimaYNishiyamaAYagiMOkaNMatsuoMMosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone productionKobe J Med Sci200753414350Search in Google Scholar

Nakamura-Pereira M, Cima LC, Llerena JC Jr, Guerra FA, Peixoto-Filho FM. Sonographic findings in a case of tetrasomy 9p associated with increased nuchal translucency and Dandy-Walker malformation. J Clin Ultrasound. 2009; 37(8): 471-474.10.1002/jcu.20612Nakamura-PereiraMCimaLCLlerenaJC JrGuerraFAPeixoto-FilhoFMSonographic findings in a case of tetrasomy 9p associated with increased nuchal translucency and Dandy-Walker malformationJ Clin Ultrasound200937847147419655321Open DOISearch in Google Scholar

Tan YQ, Chen XM, Guan XY, Lu GX. Prenatal diagnosis of nonmosaic tetrasomy 9p by microdissection and FISH: Case report. Chin Med J. [English] 2007; 120(14): 1281-1283.10.1097/00029330-200707020-00016TanYQChenXMGuanXYLuGXPrenatal diagnosis of nonmosaic tetrasomy 9p by microdissection and FISH: Case reportChin Med J. [English]20071201412811283Open DOISearch in Google Scholar

Tang W, Boyd BK, Hummel M, Wenger SL. Prenatal diagnosis of tetrasomy 9p. Am J Med Genet A. 2004; 126A(3): 328.10.1002/ajmg.a.2051115054852TangWBoydBKHummelMWengerSLPrenatal diagnosis of tetrasomy 9pAm J Med Genet A2004126A332815054852Open DOISearch in Google Scholar

Baronchelli S, Conconi D, Panzeri E, Bentivegna A, Redaelli S, Lissoni S, et al. Cytogenetics of premature ovarian failure: An investigation on 269 affected women. J Biomed Biotechnol. 2011; 2011(4): 370195. doi: 10.1155/2011/370195.21318170BaronchelliSConconiDPanzeriEBentivegnaARedaelliSLissoniSet alCytogenetics of premature ovarian failure: An investigation on 269 affected womenJ Biomed Biotechnol20112011437019510.1155/2011/370195302699521318170Search in Google Scholar

Chen CP, Lin SP, Su JW, Lee MS, Wang W. Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder. Genet Couns. 2012; 23(2): 335-338.ChenCPLinSPSuJWLeeMSWangWPhenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorderGenet Couns2012232335338Search in Google Scholar

Papoulidis I, Kontodiou M, Tzimina M, Saitis I, Hamid AB, Klein E, et al. Tetrasomy 9p mosaicism associated with a normal phenotype in two cases. Cytogenet Genome Res. 2012; 136(4): 237-241.10.1159/00033752022487875PapoulidisIKontodiouMTziminaMSaitisIHamidABKleinEet alTetrasomy 9p mosaicism associated with a normal phenotype in two casesCytogenet Genome Res2012136423724122487875Open DOISearch in Google Scholar

Podolsky R, Saltzman D, Auerbach M, Roman AS. Absent nasal bone as a marker of tetrasomy 9p. Prenat Diagn. 2011; 31(13): 1313.10.1002/pd.287722031456PodolskyRSaltzmanDAuerbachMRomanASAbsent nasal bone as a marker of tetrasomy 9pPrenat Diagn20113113131322031456Open DOISearch in Google Scholar

Wang H, Xie LS, Wang Y, Mei J. Prenatal diagnosis of mosaic tetrasomy 9p in a fetus with isolated persistent left superior vena cava. Taiwan J Obstet Gynecol. 2015; 54(2): 204-205.10.1016/j.tjog.2014.12.005WangHXieLSWangYMeiJPrenatal diagnosis of mosaic tetrasomy 9p in a fetus with isolated persistent left superior vena cavaTaiwan J Obstet Gynecol201554220420525951732Open DOISearch in Google Scholar

Sherer DM, Abramowicz JS, Jaffe R, Woods JR Jr. Cleft palate: Confirmation of prenatal diagnosis by colour Doppler ultrasound. Prenat Diagn. 1993; 13(10): 953-956.10.1002/pd.19701310098309902ShererDMAbramowiczJSJaffeRWoodsJR JrCleft palate: Confirmation of prenatal diagnosis by colour Doppler ultrasoundPrenat Diagn199313109539568309902Open DOISearch in Google Scholar

Chen CP, Chang TY, Shih JC, Lin SP, Lin CJ, Wang W, et al. Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion. Prenat Diagn. 2002; 22(12): 1063-1066.1245495910.1002/pd.459ChenCPChangTYShihJCLinSPLinCJWangWet alPrenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletionPrenat Diagn200222121063106612454959Search in Google Scholar

Hengstschläger M, Bettelheim D, Repa C, Lang S, Deutinger J, Bernaschek G, et al. A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4; 10;9). Fetal Diagn Ther. 2002; 17(4): 243-246.10.1159/000063401HengstschlägerMBettelheimDRepaCLangSDeutingerJBernaschekGet alA fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4; 10;9)Fetal Diagn Ther200217424324612065954Open DOISearch in Google Scholar

Kasakyan S, Lohmann L, Aboura A, Quimsiyeh M, Menezo Y, Tachdjian G, et al. De novo complex intra chromosomal rearrangement after ICSI: Characterisation by BACs micro array-CGH. Mol Cytogenet. 2008; 1:27.10.1186/1755-8166-1-2719105807KasakyanSLohmannLAbouraAQuimsiyehMMenezoYTachdjianGet alDe novo complex intra chromosomal rearrangement after ICSI: Characterisation by BACs micro array-CGHMol Cytogenet2008127265651119105807Open DOISearch in Google Scholar

Shehab MI, Mazen I, Bint S. Tissue-specific mosaicism for tetrasomy 9p uncovered by array CGH. Am J Med Genet A. 2011; 155A(10): 2496-2500.21998854ShehabMIMazenIBintSTissue-specific mosaicism for tetrasomy 9p uncovered by array CGHAm J Med Genet A2011155A102496250010.1002/ajmg.a.3417621998854Search in Google Scholar

Qiao YQ, Huang ML, Zheng Q, Wang Tr, Xu AT, Cao Y, et al. CNTNAP3 associated ATG16L1 expression and Crohn's disease. Mediators Inflamm. 2015; 2015(1): 404185. doi: 10.1155/2015/404185.25883416QiaoYQHuangMLZhengQWangTrXuATCaoYet alCNTNAP3 associated ATG16L1 expression and Crohn's diseaseMediators Inflamm20152015140418510.1155/2015/404185439132225883416Search in Google Scholar

Petersen OB, Vogel I, Ekelund C, Hyett J, Tabor A. Potential diagnostic consequences of applying noninvasive prenatal testing: Population-based study from a country with existing first-trimester screening. Ultrasound Obstet Gynecol. 2014; 43(3): 265-271.10.1002/uog.13270PetersenOBVogelIEkelundCHyettJTaborAPotential diagnostic consequences of applying noninvasive prenatal testing: Population-based study from a country with existing first-trimester screeningUltrasound Obstet Gynecol201443326527124375770Open DOISearch in Google Scholar

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