398 related articles for article (PubMed ID: 457430)
1. Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome?
Schinzel A
Helv Paediatr Acta; 1979 May; 34(2):141-6. PubMed ID: 457430
[TBL] [Abstract][Full Text] [Related]
2. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
Schinzel A; Schmid W
Am J Med Genet; 1980; 6(3):241-9. PubMed ID: 7424976
[TBL] [Abstract][Full Text] [Related]
3. The acrocallosal syndrome in a Turkish boy.
Yüksel M; Caliskan M; Oğur G; Ozmen M; Dolunay G; Apak S
J Med Genet; 1990 Jan; 27(1):48-9. PubMed ID: 2308155
[TBL] [Abstract][Full Text] [Related]
4. Acrocallosal syndrome: a new case.
Lungarotti MS; Marinelli D; Mezzetti D; Caputo N; Calabro A
Am J Med Genet; 1991 Jul; 40(1):94-6. PubMed ID: 1887856
[TBL] [Abstract][Full Text] [Related]
5. Acrocallosal syndrome: a case report.
Bonatz E; Descartes M; Tamarapalli JR
J Hand Surg Am; 1997 May; 22(3):492-4. PubMed ID: 9195460
[TBL] [Abstract][Full Text] [Related]
6. The acrocallosal syndrome in sisters.
Schinzel A; Kaufmann U
Clin Genet; 1986 Nov; 30(5):399-405. PubMed ID: 3802558
[TBL] [Abstract][Full Text] [Related]
7. [The acrocallosal syndrome. Report of an additional case].
Wendisch J; Lorenz P; Kabus M; Rupprecht E; Walther S
Kinderarztl Prax; 1990 Jun; 58(6):315-21. PubMed ID: 2166860
[TBL] [Abstract][Full Text] [Related]
8. A and B preaxial polydactyly with syndactyly of feet and hands in the same person--a case report.
Gawlikowska-Sroka A; Tudaj W; Czerwiński F
Adv Med Sci; 2009; 54(2):305-7. PubMed ID: 20053619
[TBL] [Abstract][Full Text] [Related]
9. Associated acral and renal malformations: a new syndrome?
Curran AS; Curran JP
Pediatrics; 1972 May; 49(5):716-25. PubMed ID: 4402497
[No Abstract] [Full Text] [Related]
10. Autosomal recessive postaxial polydactyly: report of a family.
Cantú JM; del Castillo V; Cortes R; Urrusti J
Birth Defects Orig Artic Ser; 1974; 10(5):19-22. PubMed ID: 4469981
[No Abstract] [Full Text] [Related]
11. Acrocallosal syndrome in fetus: focus on additional brain abnormalities.
Fernandez C; Soulier M; Coulibaly B; Liprandi A; Benoit B; Giuliano F; Sigaudy S; Figarella-Branger D; Fallet-Bianco C
Acta Neuropathol; 2008 Jan; 115(1):151-6. PubMed ID: 17593378
[TBL] [Abstract][Full Text] [Related]
12. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
Gnamey D; Farriaux JP
J Genet Hum; 1971 Dec; 19(4):299-316. PubMed ID: 5152131
[No Abstract] [Full Text] [Related]
13. Radiological findings in the DOOR syndrome.
Thomas PS; Nevin NC
Ann Radiol (Paris); 1982 Jan; 25(1):54-8. PubMed ID: 7065610
[No Abstract] [Full Text] [Related]
14. Schinzel acrocallosal syndrome.
Gulati S; Menon S; Kabra M; Kalra V
Indian J Pediatr; 2003 Feb; 70(2):173-6. PubMed ID: 12661815
[TBL] [Abstract][Full Text] [Related]
15. Spectrum of the acrocallosal syndrome.
Koenig R; Bach A; Woelki U; Grzeschik KH; Fuchs S
Am J Med Genet; 2002 Feb; 108(1):7-11. PubMed ID: 11857542
[TBL] [Abstract][Full Text] [Related]
16. Acrocallosal syndrome.
Shilpa BJ; Ashok L; Sattur PA
J Indian Soc Pedod Prev Dent; 2006 Mar; 24(1):45-9. PubMed ID: 16582532
[TBL] [Abstract][Full Text] [Related]
17. Unknown syndrome: mental retardation with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes' disease of the hip.
Garrett C; Tripp JH
J Med Genet; 1988 Apr; 25(4):270-2. PubMed ID: 2966861
[TBL] [Abstract][Full Text] [Related]
18. Holoprosencephaly and postaxial polydactyly with normal chromosomes. Another observation of a new malformation syndrome; a case report.
Ramaekers PR; Legius E; Verloes A; Gillerot Y; Vandenberghe K; Fryns JP
Eur J Obstet Gynecol Reprod Biol; 1990; 36(1-2):161-5. PubMed ID: 2365121
[TBL] [Abstract][Full Text] [Related]
19. Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome.
Curatolo P; Cilio MR; Del Giudice E; Romano A; Gaggero R; Pessagno A
Neuropediatrics; 1993 Apr; 24(2):77-82. PubMed ID: 8327066
[TBL] [Abstract][Full Text] [Related]
20. Four patients including two sisters with the acrocallosal syndrome (agenesis of the corpus callosum in combination with preaxial hexadactyly).
Schinzel A
Hum Genet; 1982; 62(4):382. PubMed ID: 7166318
[No Abstract] [Full Text] [Related]
[Next] [New Search]