CONGENITAL CATARACTS, RENAL TUBULAR NECROSIS AND ENCEPHALOPATHY IN TWO SISTERS

Overview

Journal Arch Dis Child

Specialty Pediatrics

Date 1963 Oct 1

PMID 14065995

Citations 3

Authors

L Crome

S Duckett

A W Franklin

Affiliations

Soon will be listed here.

Citing Articles

Genetical aspects of severe visual impairment in childhood.

Fraser G J Med Genet. 1970; 7(3):257-67.

PMID: 5312664 PMC: 1468872. DOI: 10.1136/jmg.7.3.257.

Arachnodactyly, aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones.

Bhaskar P, Jagannathan K, VALMIKINATHAN K J Neurol Neurosurg Psychiatry. 1974; 37(12):1299-1305.

PMID: 4448994 PMC: 1083643. DOI: 10.1136/jnnp.37.12.1299.

Martsolf syndrome in a brother and sister: clinical features and pattern of inheritance.

Hennekam R, van de Meeberg A, van Doorne J, Dijkstra P, Bijlsma J Eur J Pediatr. 1988; 147(5):539-43.

PMID: 3409931 DOI: 10.1007/BF00441986.

References

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