10 Articoli
Accesso libero | 25 ago 2010
A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia
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Accesso libero | 25 ago 2010
A Partial Trisomy 2p(p21→pter) Derived from a Paternal t(2;4)(p21;q33) Karyotype
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Accesso libero | 25 ago 2010
Chromatin Quality as a Crucial Factor for the Success of Fluorescent in Situ Hybridization Analyses of Unfertilized Oocytes, Polar Bodies and Arrested Zygotes
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Accesso libero | 25 ago 2010
Trisomy 21 with a Small Supernumerary Marker Chromosome Derived from Chromosomes 13/21 and 18
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Accesso libero | 25 ago 2010
Y Chromosome Single Nucleotide Polymorphisms Typing by SNaPshot MINISEQUENCING
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Accesso libero | 25 ago 2010
Unique Presentation of an 8p Deletion in a Discordant Twin with Atrioventricular Canal Defect and Prolonged Hypoglycemia
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Accesso libero | 25 ago 2010
Possible Association of Maternal Haemorrhoid with Congenital Abnormalities in their Children - a Population-Based Case-Control Study
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Accesso libero | 25 ago 2010
De Novo Duplication of Chromosome 7 (q21.1-q32); Case Report and Review of the Literature
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