✦ LIBER ✦

Multiplex PCR amplification of three microsatellites within the CFTR gene

✍ Scribed by Morral, Núria; Estivill, Xavier

Book ID: 123304629
Publisher: Elsevier Science
Year: 1992
Tongue: English
Weight: 565 KB
Volume: 13
Category: Article
ISSN: 0888-7543
DOI: 10.1016/0888-7543(92)90071-Y

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Screening Oocyte Donors for Cystic Fibro

Screening Oocyte Donors for Cystic Fibrosis Using Multiplex PCR Amplification of the CFTR Gene from Buccal Cell DNA

✍ Peter L. Chang; Steven R. Lindheim; Mark V. Sauer 📂 Article 📅 1998 🏛 Springer US 🌐 English ⚖ 182 KB

P-229 Screening oocyte donors for cystic

P-229 Screening oocyte donors for cystic fibrosis using multiplex PCR amplification of CFTR gene from buccal cell DNA

✍ P.L Chang; S.R Lindheim; E.C Ditkoff; M.V Sauer 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 125 KB

Development and multiplex PCR amplificat

Development and multiplex PCR amplification of microsatellite markers in the commercial clamVenerupis rhomboides(Mollusca: Bivalvia)

✍ Ginna Chacón, Alberto Arias-Pérez, Josefina Méndez, Ana Insua… 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 193 KB

Development and multiplex PCR amplificat

Development and multiplex PCR amplification of new microsatellite markers for the freshwater fish, ayu (Plecoglossus altivelis)

✍ HA, T. T. T. ;OKABE, M. ;MORISHIMA, K. ;NAKAYAMA, I. ;NAGASAWA, K. ;UMINO, T. 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 83 KB

New polymorphic microsatellite loci for

New polymorphic microsatellite loci for rodents of the genusMastomysusing PCR multiplexing, and cross-species amplification inMyomysandPraomys

✍ LOISEAU, A. ;KONEČNÝ, A. ;GALAN, M. ;BRYJA, J. ;COSSON, J. F. ;BROUAT, C. 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 96 KB

Fabry disease: Detection of gene rearran

Fabry disease: Detection of gene rearrangements in the human α-Galactosidase A Gene by Multiplex PCR Amplification

✍ Ruth Kornreich; Robert J. Desnick 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 360 KB

Fabry disease, an X-linked recessive disorder of glycosphingolipid catabolism, results from lesions in the alpha-galactosidase A gene leading to deficient or absent activity of the lysosomal hydrolase. To facilitate the detection of rearrangements in this 14-kb gene, a method was developed for the P