Identification of new markers in Xp21 between DXS28 (C7) and DMD

Author:

Worley K.C.,Towbin J.A.,Zhu X.M.,Barker D.F.,Ballabio A.,Chamberlain J.,Biesecker L.G.,Blethen S.L.,Brosnan P.,Fox J.E.,Rizzo W.B.,Romeo G.,Sakuragawa N.,Seltzer W.K.,Yamaguchi S.,McCabe E.R.B.

Publisher

Elsevier BV

Subject

Genetics

Reference19 articles.

1. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification;Chamberlain;Nucleic Acids Res,1988

2. Report of the committee on the genetic constitution of the X chromosome;Davies;Cytogenet. Cell Genet,1991

3. Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome;Davies;Am. J. Med. Genet,1988

4. Isolation, characterization, and physical localization of 33 human X chromosome RFLP markers;Dietz-Band;Cytogenet. Cell. Genet,1990

5. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions;Francke;Am. J. Hum. Genet,1987

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