Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome-Reference-Cited by-同舟云学术

Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome

Published:1986-03 Issue:3 Volume:72 Page:248-252
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Steinbach P.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00291888.pdf

Reference23 articles.

1. Barbi G, Steinbach P, Baur S, Vogel W (1985) Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome. Hum Genet 69:106?108

2. Camerino G, Mattei MG, Mattei JF, Jaye M, Mandel JL (1983) Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male. Nature 306:701?704

3. Daker MG, Chidiac P, Fear CN, Berry AC (1981) Fragile X a normal male: a cautionary tale. Lancet I:780

4. Evans JE, McLaren A (1985) Unborn children (protection) bill. Nature 314:127?128

5. Fishburn J, Turner G, Daniel A, Brookwell R (1983) The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers. Am J Med Genet 14:713?724

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