Detalhe da pesquisa
1.
Molecular analysis of 53 fragile X families with the probe StB12.3.
Am J Med Genet
; 53(4): 370-3, 1994 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-7864047
2.
An attempt to differentiate female relatives of Duchenne type dystrophy from healthy subjects using an automatic EMG analysis.
J Neurol Sci
; 67(1): 45-55, 1985 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-3981212
3.
"Isolated" hydrocephalus in families of spina bifida and anencephaly: a coincidence?.
Neuropediatrics
; 20(4): 220-2, 1989 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-2691919
4.
[Essential deformans osteolysis. Report of a case with progressive and generalized evolution (author's transl)]. / Ostéolyse progressive généralisée déformante. A propos d'une observation.
Chir Pediatr
; 21(6): 401-5, 1980.
Artigo
em Francês
| MEDLINE | ID: mdl-7237670
5.
X-linked hydrocephalus, with aqueductal stenosis, mental retardation, and adduction-flexion deformity of the thumbs. Report of a family.
Childs Brain
; 2(4): 226-33, 1976.
Artigo
em Inglês
| MEDLINE | ID: mdl-991665
6.
Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid gene.
Hum Mol Genet
; 2(4): 465-7, 1993 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-7684945
7.
[Paraplegia due to multiple exostoses. Report of 2 cases (author's transl)]. / Les paraplégies de la maladie des exostoses multiples. A propos de deux observations.
J Radiol Electrol Med Nucl
; 54(5): 403-7, 1973 May.
Artigo
em Francês
| MEDLINE | ID: mdl-4542698