Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome.

Author:

Borochowitz Z,Glick B,Blazer S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. The nosology of the spinal muscular atrophies;Emery, A.E.H.;Med Genet,1971

2. Mendelian inheritance in man: catalog of autosomal dominant, autosomal recessive and X-linked phenotypes;McKusick, V.A.,1989

3. International collaboration study of the spinal muscular atrophies. II. Analysis of genetic data;Emery, A.E.H.; Davie, A.M.; Holloway, S.;Neurol Sci,1976

4. Genetic studies of acute infantile spinal muscular atrophy (SMA type I): an analysis of sex ratio, segregation ratios, and sex influence;Pearn, J.A.;Med Genet,1978

5. A case of arthrogryposis multiplex congenita anatomically appearing as a foetal spinal muscular atrophy;Brandt, S.;Arch Paediatr Scand,1947

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