1.
2.
Indian J Pediatr
; 61(3): 301-6, 1994.
Artigo
em Inglês
| MEDLINE
| ID: mdl-7960007
3.
Clin Genet
; 38(3): 176-9, 1990 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-2225527
RESUMO
Five Bedouin sibs are described with Meckel-Gruber syndrome (MGS), an autosomal recessive disorder with multiple abnormalities. Each affected sib manifested only two of the three cardinal signs of MGS: occipital encephalocele and polycystic kidneys, lacking polydactyly. The phenotypic variability of the MGS pleiotropic gene is briefly discussed.
