Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study-Reference-Cited by-同舟云学术

Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study

Published:2008-04-23 Issue:1 Volume:30 Page:1-13
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Rodewald A.,Froster-Iskenius U.,Kab E.,Langenbeck U.,Schinzel A.,Schmidt A.,Schwinger E.,Steinbach P.,Veenema H.,Wegner R.-D.,Wirtz A.,Zankl H.,Zankl M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1986.tb00563.x/fullpdf

Reference21 articles.

1. Fragile X-linked mental retardation;Carpenter;Am. J. Dis. Child.,1982

2. Familial X-linked mental retardation and fragile X-chro-mosomes in two Swedish families;Gustavson;Clin. Genet.,1981

3. Familial X-linked mental retardation with a X-chromo-some abnormality;Harvey;J. Med. Genet.,1977

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Discriminant analysis of dermatoglyphic measurements in fragile X males and females;Clinical Genetics;2008-06-28

2. Dermatoglyphic peculiarities in patients with Williams-Beuren syndrome;American Journal of Medical Genetics;1994-11-15

3. Effect of fragile X on physical and intellectual traits estimated by pedigree analysis;American Journal of Medical Genetics;1993-06-01

4. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991

5. The predictive value of dermatoglyphic anomalies in the diagnosis of fra(X)-positive Martin-Bell syndrome (MBS);American Journal of Medical Genetics;1988-05