14 Artikel
Original Article
Uneingeschränkter Zugang | 28. Aug. 2019
Copy number variations in female infertility in China
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Uneingeschränkter Zugang | 28. Aug. 2019
A systematic clinical review of prenatally diagnosed tetrasomy 9p
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Uneingeschränkter Zugang | 28. Aug. 2019
Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss
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Uneingeschränkter Zugang | 28. Aug. 2019
Prenatal diagnosis of organic acidemias at a tertiary center
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Uneingeschränkter Zugang | 28. Aug. 2019
Cystic fibrosis mutation spectrum in north macedonia: A step toward personalized therapy
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Uneingeschränkter Zugang | 28. Aug. 2019
Associations between vaspin rs2236242 gene polymorphism, walking time and the risk of metabolic syndrome
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Uneingeschränkter Zugang | 28. Aug. 2019
Comparative expression analysis of human endogenous retrovirus elements in peripheral blood of children with specific language impairment
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Uneingeschränkter Zugang | 28. Aug. 2019
Janus kinase V617F mutation detection in patients with myelofibrosis
, , , und
Uneingeschränkter Zugang | 28. Aug. 2019
Novel patterns of the Epstein-Barr nuclear antigen (EBNA-1) V-Val subtype in EBV-associated nasopharyngeal carcinoma from Vietnam
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Uneingeschränkter Zugang | 28. Aug. 2019
Do fair and just systems require compensation for the disadvantages of the natural lottery? a discussion on society's duties on the provision of gene therapy
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Case Report
Uneingeschränkter Zugang | 28. Aug. 2019
Impact of genetics on neoadjuvant therapy with complete pathological response in metastatic colorectal cancer: Case report and review of the literature
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Uneingeschränkter Zugang | 28. Aug. 2019
Duplication of the SOX3 gene in an sry-negative 46,XX male with associated congenital anomalies of kidneys and the urinary tract: Case report and review of the literature
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Uneingeschränkter Zugang | 28. Aug. 2019
Achondrogenesis type 2 in a newborn with a novel mutation on the COL2A1 gene
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Uneingeschränkter Zugang | 28. Aug. 2019
A novel c.973G>T mutation in the ε-subunit of the acetylcholine receptor causing congenital myasthenic syndrome in an iranian family
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