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Results: 1 to 20 of 114

Similar articles for PubMed (Select 20717165)

1.

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. doi: 10.1038/ejhg.2010.127. Epub 2010 Aug 18. Review.

2.

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.

3.

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.

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7.

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 1;126A(1):61-7.

PMID:
15039974
8.

Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition.

Martin RA, Jones MC, Jones KL.

Am J Med Genet. 1993 Apr 15;46(2):129-31. No abstract available.

PMID:
8387244
9.

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. doi: 10.2478/v10039-009-0051-2.

PMID:
20053619
10.

[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 May-Jun;12(3):259-63. Italian.

PMID:
2177188
11.

[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. Chinese.

PMID:
14669516
12.

New type of synpolydactyly of hands and feet in two unrelated males.

Sugiura Y, Lenz W.

Am J Med Genet. 1999 Apr 23;83(5):353-5.

PMID:
10232741
13.

Congenital hypoplastic anemia in six patients: unusual association of short proximal phalanges with mild anemia.

Cetin M, Kara A, Gürgey A, Gümrük F, Irken G, Yetgin S, Altay C.

Pediatr Hematol Oncol. 1995 Mar-Apr;12(2):153-8.

PMID:
7626383
14.

Synpolydactyly of the foot in homozygotes.

Kuru I, Maralcan G, Yucel A, Aktepe F, Turkmen S, Solak M.

J Am Podiatr Med Assoc. 2006 Jul-Aug;96(4):297-304.

PMID:
16868322
15.

Sandrow syndrome of mirror hands and feet and facial abnormalities.

Kogekar N, Teebi AS, Vockley J.

Am J Med Genet. 1993 Apr 15;46(2):126-8.

PMID:
8387243
16.

An unusual family with brachydactyly.

Silva EO.

Am J Med Genet A. 2003 Mar 1;117A(2):191-3. No abstract available.

PMID:
12567422
18.

Symbrachydactyly involving hands and feet.

De Smet L, Fabry G, Fryns JP.

Genet Couns. 1998;9(1):23-7.

PMID:
9555583
19.

An acceptor splice site mutation in HOXD13 results in variable hand, but consistent foot malformations.

Kan SH, Johnson D, Giele H, Wilkie AO.

Am J Med Genet A. 2003 Aug 15;121A(1):69-74.

PMID:
12900906
20.

A large family with type IV radial polydactyly.

Seyhan A, Akarsu N, Keskin F.

J Hand Surg Br. 1998 Aug;23(4):530-3.

PMID:
9726561
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