Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome

Author:

Nakabayashi Kazuhiko,Fernandez Bridget A.,Teshima Ikuko,Shuman Cheryl,Proud Virginia K.,Curry Cynthia J.,Chitayat David,Grebe Theresa,Ming Jeffrey,Oshimura Mitsuo,Meguro Makiko,Mitsuya Kohzoh,Deb-Rinker Paromita,Herbrick Jo-Anne,Weksberg Rosanna,Scherer Stephen W.

Publisher

Elsevier BV

Subject

Genetics

Reference42 articles.

1. Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotrophins;Silver;Pediatrics,1953

2. A syndrome of intrauterine dwarfism recognizable at birth with craniofacial dysostosis, disproportionate short arms and other anomalies;Russell;Proc. R. Soc. Med.,1954

3. X-linked short stature with skin pigmentation: evidence for heterogeneity of the Russell–Silver syndrome;Partington;Clin. Genet.,1986

4. Three-generation dominant transmission of the Silver–Russell syndrome;Duncan;Am. J. Med. Genet.,1990

5. Autosomal recessive Silver–Russell syndrome;Teebi;Clin. Dysmorphol.,1992

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