Intrafamilial variation in Cohen syndrome.

Author:

Young I D,Moore J R

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference8 articles.

1. A new syndrome with hypotonia, obesity, mental deficiency and facial, oral, ocular and limb anomalies;Cohen, M.M.; Hall, B.D.; Smith, D.W.; Graham, C.B.; Lampert, K.J.;J Pediatr,1973

2. The Cohen syndrome: report of five new cases and a review of the literature;Friedman, E.; Sack, J.;J Cran Genet Dev Biol,1982

3. Further delineation of the Cohen syndrome; report on chorioretinal dystrophy, leukopenia and consanguinity;Norio, R.; Raitta, C.; Lindahl, E.;Clin Genet,1984

4. The clinical features of the Cohen sydndrome: further case reports;MA, North C.Patton; M, Baraitser; RM, Winter;J Med Genet,1985

5. Cohen syndrome with bull's eye macular lesion;Resnick, K.; Zuckerrnan, J.; Cotlier, E.;Ophthalmic Paediatr Genet,1986

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