✦ LIBER ✦

A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3

✍ Scribed by Annick Cabot; Jean-Michel Rozet; Sylvie Gerber; Isabelle Perrault; Dominique Ducroq; Asmae Smahi; Eric Souied; Arnold Munnich; Josseline Kaplan

Book ID: 117852772
Publisher: American Society of Human Genetics
Year: 1999
Tongue: English
Weight: 641 KB
Volume: 64
Category: Article
ISSN: 0002-9297
DOI: 10.1086/302324

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Gene for X-Linked Optic Atrophy Is Clo

A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome

✍ Jacqueline J.M. Assink; Nel T. Tijmes; Jacoline B. ten Brink; Roelof-Jan Oostra; 📂 Article 📅 1997 🏛 American Society of Human Genetics 🌐 English ⚖ 103 KB

Assignment of the gene for complete X-li

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3

✍ Musarella, M.A.; Weleber, R.G.; Murphey, W.H.; Young, R.S.L.; Anson-Cartwright, 📂 Article 📅 1989 🏛 Elsevier Science 🌐 English ⚖ 999 KB

Development of a 1.4-Mb BAC/PAC Contig a

Development of a 1.4-Mb BAC/PAC Contig and Physical Map within the Critical Region for Complete X-Linked Congenital Stationary Night Blindness in Xp11.4

✍ R.L. Sparkes; C.G. Summer; K.M. Boycott; R.J. Zahorchak; N.T. Bech-Hansen 📂 Article 📅 2000 🏛 Elsevier Science 🌐 English ⚖ 62 KB

Remapping of the RP15 Locus for X-Linked

Remapping of the RP15 Locus for X-Linked Cone-Rod Degeneration to Xp11.4-p21.1, and Identification of a De Novo Insertion in the RPGR Exon ORF15

✍ Alan J. Mears; Suja Hiriyanna; Raf Vervoort; Beverly Yashar; Linn Gieser; Stacey 📂 Article 📅 2000 🏛 American Society of Human Genetics 🌐 English ⚖ 864 KB