308 related articles for article (PubMed ID: 7666393)
1. A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data.
Sayli BS; Akarsu AN; Sayli U; Akhan O; Ceylaner S; Sarfarazi M
J Med Genet; 1995 Jun; 32(6):421-34. PubMed ID: 7666393
[TBL] [Abstract][Full Text] [Related]
2. A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?
Akarsu AN; Akhan O; Sayli BS; Sayli U; Baskaya G; Sarfarazi M
J Med Genet; 1995 Jun; 32(6):435-41. PubMed ID: 7666394
[TBL] [Abstract][Full Text] [Related]
3. [Genetic analysis of a Chinese pedigree with congenital synpolydactyly].
Qin W; Shu AL; Xing QH; Yang MS; Feng GY; He L
Yi Chuan Xue Bao; 2003 Oct; 30(10):973-7. PubMed ID: 14669516
[TBL] [Abstract][Full Text] [Related]
4. Type II familial synpolydactyly: report on two families with an emphasis on variations of expression.
Al-Qattan MM
Eur J Hum Genet; 2011 Jan; 19(1):112-4. PubMed ID: 20717165
[TBL] [Abstract][Full Text] [Related]
5. A large family with type IV radial polydactyly.
Seyhan A; Akarsu N; Keskin F
J Hand Surg Br; 1998 Aug; 23(4):530-3. PubMed ID: 9726561
[TBL] [Abstract][Full Text] [Related]
6. Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?
Percin EF; Percin S; Egilmez H; Sezgin I; Ozbas F; Akarsu AN
J Med Genet; 1998 Oct; 35(10):868-74. PubMed ID: 9783716
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Synpolydactyly of the foot in homozygotes.
Kuru I; Maralcan G; Yucel A; Aktepe F; Turkmen S; Solak M
J Am Podiatr Med Assoc; 2006; 96(4):297-304. PubMed ID: 16868322
[TBL] [Abstract][Full Text] [Related]
10. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
Majewski E; Goecke T; Meinecke P
Am J Med Genet; 1996 May; 63(1):185-9. PubMed ID: 8723107
[TBL] [Abstract][Full Text] [Related]
11. A hereditable combination of congenital anomalies.
Agarwal RP; Jain D; Ramesh Babu CS; Garg RK
J Bone Joint Surg Br; 1996 May; 78(3):492-4. PubMed ID: 8636194
[TBL] [Abstract][Full Text] [Related]
12. Polydactyly: a study of four generations of a Turkish family including an affected member with bilateral cleft lip and palate.
Koçer U; Aksoy HM; Tiftikcioğlu YO; Karaaslan O
Scand J Plast Reconstr Surg Hand Surg; 2002; 36(5):284-8. PubMed ID: 12477087
[TBL] [Abstract][Full Text] [Related]
13. Complex Camptosynpolydactyly and Mesoaxial synostotic syndactyly with phalangeal reduction are allelic disorders.
Phadke SR; Kar A; Bhowmik AD; Dalal A
Am J Med Genet A; 2016 Jun; 170(6):1622-5. PubMed ID: 27041388
[TBL] [Abstract][Full Text] [Related]
14. Hypoplastic synpolydactyly as a new clinical subgroup of synpolydactyly.
Kuru I; Samli H; Yucel A; Bozan ME; Turkmen S; Solak M
J Hand Surg Br; 2004 Dec; 29(6):614-20. PubMed ID: 15542226
[TBL] [Abstract][Full Text] [Related]
15. Synpolydactyly (type II syndactyly) with aplasia/hypoplasia of the middle phalanges of the toes: report on a family with eight affected members in four generations.
Camera G; Camera A; Pozzolo S; Costa M; Mantero R
Am J Med Genet; 1995 Jan; 55(2):244-6. PubMed ID: 7717427
[TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant syndrome of camptodactyly, clinodactyly, syndactyly, and bifid toes.
Malik S; Afzal M; Gul S; Wahab A; Ahmad M
Am J Med Genet A; 2010 Sep; 152A(9):2313-7. PubMed ID: 20683984
[TBL] [Abstract][Full Text] [Related]
17. [Synpolydactyly: unusual features and variable expression in 5 generations of an Italian family].
Chessa Ricotti G; Lapi E; De Bernardi A; Corti P
Pediatr Med Chir; 1990; 12(3):259-63. PubMed ID: 2177188
[TBL] [Abstract][Full Text] [Related]
18. Polydactyly, postaxial, type B.
Holmes LB; Nasri H; Hunt AT; Toufaily MH; Westgate MN
Birth Defects Res; 2018 Jan; 110(2):134-141. PubMed ID: 29377639
[TBL] [Abstract][Full Text] [Related]
19. A novel insertion and deletion mutation in the BHLHA9 underlies polydactyly and mesoaxial synostotic syndactyly with phalangeal reduction.
Ullah A; Ali RH; Majeed AI; Liaqat K; Shah PW; Khan B; Bilal M; Umair M; Ahmad W
Eur J Med Genet; 2019 Apr; 62(4):278-281. PubMed ID: 30107244
[TBL] [Abstract][Full Text] [Related]
20. A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin.
Malik S; Arshad M; Amin-Ud-Din M; Oeffner F; Dempfle A; Haque S; Koch MC; Ahmad W; Grzeschik KH
Am J Med Genet A; 2004 Apr; 126A(1):61-7. PubMed ID: 15039974
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
