These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. Polydactyly of the foot: an analysis of 265 cases and a morphological classification. Watanabe H; Fujita S; Oka I Plast Reconstr Surg; 1992 May; 89(5):856-77. PubMed ID: 1561258 [TBL] [Abstract][Full Text] [Related]
5. Parental consanguinity in specific types of congenital anomalies. Rittler M; Liascovich R; López-Camelo J; Castilla EE Am J Med Genet; 2001 Jul; 102(1):36-43. PubMed ID: 11471170 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Postaxial polydactyly, ulnar ray dysgenesis, and renal cystic dysplasia in sibs. Kaplan BS; Bellah RD Am J Med Genet; 1999 Dec; 87(5):426-9. PubMed ID: 10594882 [TBL] [Abstract][Full Text] [Related]
8. An unusual case of preaxial polydactyly of the hands and feet: a case report. Al-Qattan MM; Hashem FK; Al Malaq A J Hand Surg Am; 2002 May; 27(3):498-502. PubMed ID: 12015726 [TBL] [Abstract][Full Text] [Related]
9. Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome. Lohan S; Spielmann M; Doelken SC; Flöttmann R; Muhammad F; Baig SM; Wajid M; Hülsemann W; Habenicht R; Kjaer KW; Patil SJ; Girisha KM; Abarca-Barriga HH; Mundlos S; Klopocki E Clin Genet; 2014 Oct; 86(4):318-25. PubMed ID: 24456159 [TBL] [Abstract][Full Text] [Related]
10. A novel EZH2 gene variant in a case of Weaver syndrome with postaxial polydactyly. Turkkahraman D; Sakarya ANP; Randa NC Am J Med Genet A; 2021 Jul; 185(7):2234-2237. PubMed ID: 33788986 [No Abstract] [Full Text] [Related]
11. Clinical and descriptive genetic study of polydactyly: a Pakistani experience of 313 cases. Malik S; Ullah S; Afzal M; Lal K; Haque S Clin Genet; 2014 May; 85(5):482-6. PubMed ID: 23772746 [TBL] [Abstract][Full Text] [Related]
12. Hand and foot postaxial polydactyly: two different traits. Castilla EE; da Graca Dutra M; Lugarinho da Fonseca R; Paz JE Am J Med Genet; 1997 Nov; 73(1):48-54. PubMed ID: 9375922 [TBL] [Abstract][Full Text] [Related]
13. Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family. Kantaputra PN; Chalidapong P Am J Med Genet; 2000 Jul; 93(2):126-31. PubMed ID: 10869115 [TBL] [Abstract][Full Text] [Related]
14. Upper limb malformations in DiGeorge syndrome. Cormier-Daire V; Iserin L; Théophile D; Sidi D; Vervel C; Padovani JP; Vekemans M; Munnich A; Lyonnet S Am J Med Genet; 1995 Mar; 56(1):39-41. PubMed ID: 7747784 [TBL] [Abstract][Full Text] [Related]
15. Terminal limb congenital malformations: analysis of 523 cases. Masada K; Tsuyuguchi Y; Kawabata H; Kawai H; Tada K; Ono K J Pediatr Orthop; 1986; 6(3):340-5. PubMed ID: 3711327 [TBL] [Abstract][Full Text] [Related]
16. A case of bilateral dysplasia epiphysealis hemimelica associated with polydactyly and syndactyly. Takegami Y; Nogami H Clin Orthop Relat Res; 1993 Nov; (296):307-9. PubMed ID: 8222443 [TBL] [Abstract][Full Text] [Related]
17. Classification of postaxial polydactyly of the foot. Lee HS; Park SS; Yoon JO; Kim JS; Youm YS Foot Ankle Int; 2006 May; 27(5):356-62. PubMed ID: 16701056 [TBL] [Abstract][Full Text] [Related]
18. A rare case of unilateral postaxial duplicated foot in a developmentally normal child. Sahdi H; Hoong CW; Rasit AH; Arianto F; Siong LK; Abdullah NA J Orthop Surg (Hong Kong); 2017 Jan; 25(1):2309499016684989. PubMed ID: 28166702 [TBL] [Abstract][Full Text] [Related]
19. Complex postaxial polydactyly types A and B with camptodactyly, hypoplastic third toe, zygodactyly and other digit anomalies caused by a novel GLI3 mutation. Mumtaz S; Yıldız E; Lal K; Tolun A; Malik S Eur J Med Genet; 2017 May; 60(5):268-274. PubMed ID: 28315472 [TBL] [Abstract][Full Text] [Related]
20. Probable new syndrome in a Mexican family with congenital palmar polyonychia and postaxial limb defects. Román Corona-Rivera J; Corona-Rivera E; Fragoso-Herrera R; Nuño-Arana I; Loera-Castañeda V Am J Med Genet A; 2004 Mar; 125A(2):205-9. PubMed ID: 14981725 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]