Integrated STS/YAC Physical, Genetic, and Transcript Map of Human Xq21.3 to q23/q24 (DXS1203

Integrated STS/YAC Physical, Genetic, and Transcript Map of Human Xq21.3 to q23/q24 (DXS1203–DXS1059)

Published:1999-06 Issue:2 Volume:58 Page:188-201
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Srivastava Anand K.,McMillan Sandra,Jermak Christopher,Shomaker Michael,Copeland-Yates Susan A.,Sossey-Alaoui Khalid,Mumm Steven,Schlessinger David,Nagaraja Ramaiah

Publisher

Elsevier BV

Subject

Genetics

Reference70 articles.

1. Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents;Albertsen;Proc. Natl. Acad. Sci. USA,1990

2. PAK3 mutation in nonsyndromic X-linked mental retardation;Allen;Nat. Genet.,1998

3. A YAC contig in Xq22.3–q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3;Allen;Genomics,1998

4. A 3.5 genome equivalent multi access YAC library: Construction, characterisation, screening and storage;Anand;Nucleic Acids Res.,1990

5. Identification of mutations in the COL4A5 collagen gene in Alport syndrome;Barker;Science,1990

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