✦ LIBER ✦

BMP15 mutations in XX gonadal dysgenesis and premature ovarian failure

✍ Scribed by Susanne Ledig; Albrecht Röpke; Gabriele Haeusler; Bernd Hinney; Peter Wieacker

Book ID: 113432362
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 356 KB
Volume: 198
Category: Article
ISSN: 1097-6868
DOI: 10.1016/j.ajog.2007.05.029

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

BMP15 and premature ovarian failure: cau

BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms?

✍ Besma Lakhal; Paul Laissue; Rim Braham; Hatem Elghezal; Ali Saâd; Marc Fellous; 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 57 KB

Mutations and sequence variants in GDF9

Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

✍ Laissue, P. 📂 Article 📅 2006 🏛 Bioscientifica 🌐 English ⚖ 178 KB

Copy Number Variants in Premature Ovaria

Copy Number Variants in Premature Ovarian Failure and Ovarian Dysgenesis

✍ Ledig, S.; Röpke, A.; Wieacker, P. 📂 Article 📅 2010 🏛 S. Karger AG 🌐 English ⚖ 314 KB

Mutational analysis of BMP15 and GDF9 as

Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure

✍ Ashwini L. Chand; Anna P. Ponnampalam; Sarah E. Harris; Ingrid M. Winship; Andre 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 92 KB

Gene analysis in patients with premature

Gene analysis in patients with premature ovarian failure or gonadal dysgenesis: A preliminary study

✍ Ana Maria Massad-Costa; Ismael Dale Cotrim Guerreiro da Silva; Regina Affonso; J 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 413 KB

Gonadal (ovarian) dysgenesis in 46,XX in

Gonadal (ovarian) dysgenesis in 46,XX individuals: Frequency of the autosomal recessive form

✍ Meyers, Carole M.; Boughman, Joann A.; Rivas, Marian; Wilroy, R. Sidney; Simpson 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 29 KB 👁 2 views

Gonadal (ovarian) dysgenesis with normal chromosomes (46,XX) clearly is a heterogeneous condition. In some forms, the defect is restricted to the gonads, whereas other affected females show neurosensory hearing loss (Perrault syndrome). In another form, brothers may have germ cell aplasia [Granat et