The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs
- PMID: 1173820
- DOI: 10.1016/s0022-3476(75)80074-6
The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs
Similar articles
-
Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.Genet Couns. 2011;22(1):55-61. Genet Couns. 2011. PMID: 21614989
-
Aplasia cutis congenita of the scalp, skull and dura associated with Adams-Oliver syndrome.Turk Neurosurg. 2008 Apr;18(2):191-3. Turk Neurosurg. 2008. PMID: 18597236
-
[The Adams-Oliver syndrome in Spain: the epidemiological aspects].An Esp Pediatr. 1996 Jul;45(1):57-61. An Esp Pediatr. 1996. PMID: 8849132 Spanish.
-
Aplasia cutis congenita: a clinical review and associated defects.Neonatal Netw. 1992 Oct;11(7):17-27. Neonatal Netw. 1992. PMID: 1406547 Review. No abstract available.
-
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects.Am J Med Genet A. 2009 Aug;149A(8):1860-81. doi: 10.1002/ajmg.a.32708. Am J Med Genet A. 2009. PMID: 19610107 Review.
Cited by
-
Congenital scalp defects with distal limb anomalies: report of a family.J Med Genet. 1976 Dec;13(6):466-8. doi: 10.1136/jmg.13.6.466. J Med Genet. 1976. PMID: 1018305 Free PMC article.
-
Congenital scalp defect with distal limb reduction anomalies.Eur J Pediatr. 1977 Nov 4;126(4):289-95. doi: 10.1007/BF00477056. Eur J Pediatr. 1977. PMID: 201465
-
Congenital scalp and skull defects with terminal transverse limb anomalies (Adams-Oliver syndrome): report of three additional cases.Eur J Pediatr. 1990 May;149(8):565-6. doi: 10.1007/BF01957693. Eur J Pediatr. 1990. PMID: 2161342 Review.
-
Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome.Eur J Pediatr. 1976 Apr 6;122(1):19-55. doi: 10.1007/BF00445030. Eur J Pediatr. 1976. PMID: 1261566
-
Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance.Hum Genet. 1985;71(1):86-8. doi: 10.1007/BF00295675. Hum Genet. 1985. PMID: 4029956
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources