110 related articles for article (PubMed ID: 11520023)
1. Familial torticollis with polydactyly: manifestation in three generations.
Hosalkar H; Gill IS; Gujar P; Shaw BA
Am J Orthop (Belle Mead NJ); 2001 Aug; 30(8):656-8. PubMed ID: 11520023
[TBL] [Abstract][Full Text] [Related]
2. Familial congenital muscular torticollis: case report and review of the literature.
Thompson F; McManus S; Colville J
Clin Orthop Relat Res; 1986 Jan; (202):193-6. PubMed ID: 3955948
[TBL] [Abstract][Full Text] [Related]
3. Genetical and epidemiological studies of polydactyly in Hungary.
Bellovits O
Anthropol Anz; 2003 Dec; 61(4):413-9. PubMed ID: 14717534
[TBL] [Abstract][Full Text] [Related]
4. Holt-Oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family.
Moens P; De Smet L; Fabry G; Fryns JP
Genet Couns; 1993; 4(4):277-80. PubMed ID: 8110414
[No Abstract] [Full Text] [Related]
5. Sporadic familial polydactyly.
Karaaslan O; Tiftikcioglu YO; Aksoy HM; Kocer U
Genet Couns; 2003; 14(4):401-5. PubMed ID: 14738113
[TBL] [Abstract][Full Text] [Related]
6. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
Kang S; Graham JM; Olney AH; Biesecker LG
Nat Genet; 1997 Mar; 15(3):266-8. PubMed ID: 9054938
[TBL] [Abstract][Full Text] [Related]
7. Bilateral preaxial polydactyly: a possible dominant inheritant.
Nishikawa M; Bitoh N; Kikkawa F; Horii E; Mizutani S
Arch Gynecol Obstet; 2003 Oct; 268(4):337-9. PubMed ID: 14504883
[TBL] [Abstract][Full Text] [Related]
8. Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature.
Küster W; Lenz W; Kääriäinen H; Majewski F
Am J Med Genet; 1988 Sep; 31(1):99-115. PubMed ID: 3066221
[TBL] [Abstract][Full Text] [Related]
9. Congenital muscular torticollis: is heredity a possible factor in a family with five torticollis patients in three generations?
Engin C; Yavuz SS; Sahin FI
Plast Reconstr Surg; 1997 Apr; 99(4):1147-50. PubMed ID: 9091917
[TBL] [Abstract][Full Text] [Related]
10. Postaxial polydactyly type A/B (PAP-A/B) is linked to chromosome 19p13.1-13.2 in a Chinese kindred.
Zhao H; Tian Y; Breedveld G; Huang S; Zou Y; Y J; Chai J; Li H; Li M; Oostra BA; Lo WH; Heutink P
Eur J Hum Genet; 2002 Mar; 10(3):162-6. PubMed ID: 11973619
[TBL] [Abstract][Full Text] [Related]
11. Familial crossed polysyndactyly.
Goldstein DJ; Kambouris M; Ward RE
Am J Med Genet; 1994 Apr; 50(3):215-23. PubMed ID: 8042663
[TBL] [Abstract][Full Text] [Related]
12. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.
Tsukurov O; Boehmer A; Flynn J; Nicolai JP; Hamel BC; Traill S; Zaleske D; Mankin HJ; Yeon H; Ho C
Nat Genet; 1994 Mar; 6(3):282-6. PubMed ID: 8012391
[TBL] [Abstract][Full Text] [Related]
13. Absent tibiae--polydactyly--triphalangeal thumbs with fibular dimelia: variable expression of the Werner (McKusick 188770) syndrome?
Vargas FR; Pontes RL; Llerena Júnior JC; de Almeida JC
Am J Med Genet; 1995 Jan; 55(3):261-4. PubMed ID: 7726219
[TBL] [Abstract][Full Text] [Related]
14. Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new case.
Garavelli L; Guareschi E; Errico S; Simoni A; Bergonzini P; Zollino M; Gurrieri F; Mancini GM; Schot R; Van Der Spek PJ; Frigieri G; Zonari P; Albertini E; Giustina ED; Amarri S; Banchini G; Dobyns WB; Neri G
Neuropediatrics; 2007 Aug; 38(4):200-3. PubMed ID: 18058629
[TBL] [Abstract][Full Text] [Related]
15. Thumb/hallux duplication and preaxial polydactyly type I.
Orioli IM; Castilla EE
Am J Med Genet; 1999 Jan; 82(3):219-24. PubMed ID: 10215544
[TBL] [Abstract][Full Text] [Related]
16. [Hypoplasia of the tibia, polydactyly, and triphalangeal thumb: 1st family described in Venezuela].
Martínez-Basalo C; González-Inciarte ME; Delgado-Luengo W; Casilla-Nava S; González-Incíarte L; Alvarez-Nava F; Boscán-Porras N; Delgado-Luengo J
Invest Clin; 1997 Dec; 38(4):219-26. PubMed ID: 9527389
[TBL] [Abstract][Full Text] [Related]
17. [Polydactyly: a genetic epidemiological study in Santiago, Chile].
Cifuentes L; Nazer J; Hüber ME; Ramírez R; Nazer C; Morales I
Rev Med Chil; 1996 Mar; 124(3):313-8. PubMed ID: 9008943
[TBL] [Abstract][Full Text] [Related]
18. Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: a rare brain malformation syndrome associated with mental retardation and seizures.
Mirzaa G; Dodge NN; Glass I; Day C; Gripp K; Nicholson L; Straub V; Voit T; Dobyns WB
Neuropediatrics; 2004 Dec; 35(6):353-9. PubMed ID: 15627943
[TBL] [Abstract][Full Text] [Related]
19. Epidemiological analysis of rare polydactylies.
Castilla EE; Lugarinho da Fonseca R; da Graca Dutra M; Bermejo E; Cuevas L; Martínez-Frías ML
Am J Med Genet; 1996 Nov; 65(4):295-303. PubMed ID: 8923939
[TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
Guttmacher AE
Am J Med Genet; 1993 Apr; 46(2):219-22. PubMed ID: 8484413
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
