Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers.

Author:

Martinez F,Tomas M,Millan J M,Fernandez A,Palau F,Prieto F

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference19 articles.

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2. The 1993-94 Genethon human genetic linkage map;Gyapay, G.; Morissette, J.; Vignal, A.;Nat Genet,1994

3. Characterization of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) loci;Gedeon, A.K.; Holman, K.; Richards, R.I.; Mulley, J.C.;Am 7 Med Genet,1992

4. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms;Clemens, P.R.; Fenwick, R.G.; Chamberlain, J.S.;AmJ Hum Genet,1991

5. Dinucleotide repeat polymorphism at the MAOA locus;Black, G.; Chen, Z.Y.; Craig, I.; Powell, J.;Nucleic Acids Res,1991

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