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Clinical Dysmorphology

Volumn 6, Issue 1, 1997, Pages 39-44

New syndrome or severe expression of Gordon syndrome? A case report

(4) Courtens, W a Perlmutter, N b Dan, B b Vamos, E a

a BRUGMANN UNIVERSITY HOSPITAL (Belgium)

b HOP UNIV DES ENFANTS REINE FABIOLA (Belgium)

Author keywords

autosomal dominant or X linked inheritance; cleft palate; failure to thrive; hearing loss; hypotonia

Indexed keywords

ARTHROGRYPOSIS; ARTICLE; CAMPTODACTYLY; CASE REPORT; CHILD; CLEFT PALATE; HUMAN; MALE; MALFORMATION SYNDROME; MUSCLE HYPOTONIA; PRIORITY JOURNAL; SYNDROME DELINEATION;

EID: 0031032462 PISSN: 09628827 EISSN: None Source Type: Journal
DOI: 10.1097/00019605-199701000-00007 Document Type: Article

Times cited : (6)

References (11)

1
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2
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- Camptodactyly, cleft palate and club foot (the Gordon syndrome) - A report of a large pedigree
- Halal F, Fraser FC (1979): Camptodactyly, cleft palate and club foot (the Gordon syndrome) - a report of a large pedigree. J Med Genet 16: 149-150.
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- Halal, F.¹ Fraser, F.C.²

3
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- The distal arthrogryposes: Delineation of new entities - Review and nosologic discussion
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4
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- A second family with cleft palate, club feet and camptodactyly
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- (1972) Am J Hum Genet , vol.24
- Higgins, J.V.¹ Hackel, E.² Kapur³

5
- 0022901513
- Peculiar face, deafness, cleft palate, male pseudohermaphroditism, and growth and psychomotor retardation; a new autosomal recessive syndrome?
- Ieshima A, Koeda T, Inagaki M (1986): Peculiar face, deafness, cleft palate, male pseudohermaphroditism, and growth and psychomotor retardation; a new autosomal recessive syndrome? Clin Genet 30: 136-141.
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- Ieshima, A.¹ Koeda, T.² Inagaki, M.³

6
- 0021922929
- Brief clinical report: An unusual distal arthrogryposis
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7
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- Autosomal dominant inheritance of distal arthrogryposis
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8
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- Distal arthrogryposis type II: A family with varying congenital abnormalities
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9
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- The Gordon syndrome: Autosomal dominant cleft palate, camptodactyly, and club feet
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10
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11
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- The Gordon syndrome
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.