87 related articles for article (PubMed ID: 3216192)
1. [Holoprosencephaly, polydactyly, cardiopathy: new syndrome or a new case of hydrolethalus?].
André SA; Cordier MP; Beaufrère AM; Guillaud M; Robert JM
J Genet Hum; 1988 Dec; 36(5):463-8. PubMed ID: 3216192
[TBL] [Abstract][Full Text] [Related]
2. [Renal hypoplasia, polydactyly, cardiopathy: a new syndrome?].
Bonnet J; Cordier MP; Ollagnon E; Guillaud MH; Raudrant D; Robert JM; Charvet F
J Genet Hum; 1987 Aug; 35(4):279-89. PubMed ID: 3309184
[TBL] [Abstract][Full Text] [Related]
3. Familial holoprosencephaly, heart defects, and polydactyly.
Hennekam RC; van Noort G; de la Fuente AA
Am J Med Genet; 1991 Nov; 41(2):258-62. PubMed ID: 1785646
[TBL] [Abstract][Full Text] [Related]
4. Holoprosencephaly and polydactyly: a possible expression of the hydrolethalus syndrome.
Bachman H; Clark RD; Salahi W
J Med Genet; 1990 Jan; 27(1):50-2. PubMed ID: 2407847
[TBL] [Abstract][Full Text] [Related]
5. Hydrolethalus (Salonen-Herva-Norio) syndrome: further clinicopathological delineation.
Anyane-Yeboa K; Collins M; Kupsky W; Maidman J; Malin J; Yeh M
Am J Med Genet; 1987 Apr; 26(4):899-907. PubMed ID: 3296755
[TBL] [Abstract][Full Text] [Related]
6. "Holoprosencephaly-polydactyly" (pseudotrisomy 13) syndrome: expansion of the phenotypic spectrum.
Lurie IW; Wulfsberg EA
Am J Med Genet; 1993 Sep; 47(3):405-9. PubMed ID: 8135289
[TBL] [Abstract][Full Text] [Related]
7. [Postaxial polydactyly in a female neonate associated with hydrocolpos due to vaginal atresia and with a congenital cardiopathy: the McKusick-Kaufman syndrome].
Castel Y; Toudic L; Alix D; Le Guern H; Colin A
J Genet Hum; 1982 Nov; 30(4):329-37. PubMed ID: 7169598
[TBL] [Abstract][Full Text] [Related]
8. [Kaufmann syndrome or VACTERL association? Discussion of a differential diagnosis].
Dodinval P; Daemers G; Legat C
J Genet Hum; 1984 Jun; 32(2):129-36. PubMed ID: 6736938
[TBL] [Abstract][Full Text] [Related]
9. [Prenatal diagnosis of holoprosencephaly with postaxial polydactyly, cardiopathy with normal karyotype].
Salamanca A; Padilla MC; Sabatel RM; Motos MA; Stemper K; Gonzalez-Gomez F
Geburtshilfe Frauenheilkd; 1992 Dec; 52(12):783-5. PubMed ID: 1490560
[TBL] [Abstract][Full Text] [Related]
10. Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.
Verloes A; Aymé S; Gambarelli D; Gonzales M; Le Merrer M; Mulliez N; Philip N; Roume J
J Med Genet; 1991 May; 28(5):297-303. PubMed ID: 1865466
[TBL] [Abstract][Full Text] [Related]
11. A new case of megalencephaly and perisylvian polymicrogyria with post-axial polydactyly and hydrocephalus: MPPH syndrome.
Colombani M; Chouchane M; Pitelet G; Morales L; Callier P; Pinard JP; Lion-François L; Thauvin-Robinet C; Mugneret F; Huet F; Guibaud L; Faivre L
Eur J Med Genet; 2006; 49(6):466-71. PubMed ID: 16807158
[TBL] [Abstract][Full Text] [Related]
12. Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly.
Young ID; Madders DJ
J Med Genet; 1987 Nov; 24(11):714-5. PubMed ID: 3430550
[TBL] [Abstract][Full Text] [Related]
13. Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes.
Dincsoy MY; Salih MA; al-Jurayyan N; al Saadi M; Patel PJ
Am J Med Genet; 1995 Apr; 56(3):317-21. PubMed ID: 7778599
[TBL] [Abstract][Full Text] [Related]
14. Severe form of hypoglossia-hypodactylia syndrome associated with complex cardiopathy: a case report.
Elalaoui SC; Ratbi I; Malih M; Bounasse M; Sefiani A
Int J Pediatr Otorhinolaryngol; 2010 Sep; 74(9):1092-4. PubMed ID: 20637513
[TBL] [Abstract][Full Text] [Related]
15. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
Sivasli O; Ozer EA; Ozer A; Aydinlioglu H; Helvaci M
Genet Couns; 2007; 18(2):247-50. PubMed ID: 17710878
[TBL] [Abstract][Full Text] [Related]
16. Brief clinical report: familial neonatally lethal syndrome of hypoplastic left heart, absent pulmonary lobation, polydactyly, and talipes, probably Smith-Lemli-Opitz (RSH) syndrome.
Kohler HG
Am J Med Genet; 1983 Mar; 14(3):423-8. PubMed ID: 6859093
[TBL] [Abstract][Full Text] [Related]
17. [Hydrometrocolpos, polydactylia and congenital heart defect (the McKusick-Dungy-Kaufman syndrome)].
Hamel BC; ter Haar BG
Tijdschr Kindergeneeskd; 1984 Aug; 52(4):129-33. PubMed ID: 6495304
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease.
Franceschini P; Vardeu MP; Signorile F; Testa A; Guala A; Franceschini D; Dalforno L
Am J Med Genet; 1993 May; 46(3):341-4. PubMed ID: 8488882
[TBL] [Abstract][Full Text] [Related]
20. Further delineation of pseudotrisomy 13 syndrome: a case without polydactyly.
Ramos-Arroyo MA; de Miguel C; Valiente A; Moreno-Laguna S
Am J Med Genet; 1994 Apr; 50(2):177-9. PubMed ID: 8010349
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
