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Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader–Willi and Angelman syndromes

✍ Scribed by Flori, Elisabeth; Biancalana, Valérie; Girard-Lemaire, Françoise; Favre, Romain; Flori, Jean; Doray, Bérénice; Louis Mandel, Jean


Book ID
110025543
Publisher
Nature Publishing Group
Year
2003
Tongue
English
Weight
158 KB
Volume
12
Category
Article
ISSN
1018-4813

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