Human monoamine oxidase gene (MAOA): Chromosome position (Xp21-p11) and DNA polymorphism

Author:

Ozelius Laurie,Hsu Yun-Pung P.,Bruns Gail,Powell John F.,Chen Shiuan,Weyler Walter,Utterback Margot,Zucker Deborah,Haines Jonathan,Trofatter James A.,Conneally P.Michael,Gusella James F.,Breakefield Xandra O.

Publisher

Elsevier BV

Subject

Genetics

Reference44 articles.

1. A strategy to reveal high-frequency RFLPs along the human X chromosome;Aldridge;Amer. J. Hum. Genet,1984

2. Molecular cloning of human monoamine oxidase A and B;Bach;FEBS,1988

3. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs;Bakker;Lancet,1985

4. Linkage analysis in a family with dominantly inherited torsion dystonia: Exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms;Breakefield;J. Neurogenet,1986

5. Isolation of X chromosome DNA sequences;Bruns;Adv. Exp. Med. Biol,1982

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