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Similar articles for PubMed (Select 8484413)

1.

Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.

Guttmacher AE.

Am J Med Genet. 1993 Apr 15;46(2):219-22.

PMID:
8484413
2.

An Indian family with postaxial polydactyly in four generations.

Kucheria K, Kenue RK, Taneja N.

Clin Genet. 1981 Jul;20(1):36-9.

PMID:
7296946
3.

A postaxial polydactyly and progressive myopia syndrome of autosomal dominant origin.

Czeizel A, Brooser G.

Clin Genet. 1986 Nov;30(5):406-8.

PMID:
3802559
4.

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
5.

Crossed polydactyly type I in a mother and son: an autosomal dominant trait?

Ishikiriyama S, Sawada H, Nambu H, Niikawa N.

Am J Med Genet. 1991 Jul 1;40(1):41-3.

PMID:
1887848
6.

Polydactyly: a study of a five generation Indian family.

Radhakrishna U, Multani AS, Solanki JV, Shah VC, Chinoy NJ.

J Med Genet. 1993 Apr;30(4):296-9.

7.

Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritance.

Silengo MC, Biagioli M, Bell GL, Bona G, Franceschini P.

Clin Genet. 1987 Jan;31(1):13-8.

PMID:
3568429
8.

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. Epub 2002 Nov 16.

PMID:
14504883
9.

Acrocallosal syndrome: a case report.

Bonatz E, Descartes M, Tamarapalli JR.

J Hand Surg Am. 1997 May;22(3):492-4.

PMID:
9195460
10.

The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.

Gollop TR, Fontes LR.

Am J Med Genet. 1985 Sep;22(1):59-68. Review.

PMID:
3901752
12.

Autosomal recessive postaxial polydactyly: report of a family.

Cantú JM, del Castillo V, Cortes R, Urrusti J.

Birth Defects Orig Artic Ser. 1974;10(5):19-22. No abstract available.

PMID:
4469981
13.

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.

14.

Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome.

Curry CJ, Hall BD.

Birth Defects Orig Artic Ser. 1979;15(5B):253-63. No abstract available.

PMID:
526581
15.

Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome?

Majewski F, Stöss H, Goecke T, Kemperdick H.

Hum Genet. 1983;65(2):125-33.

PMID:
6654326
16.

Clinical aspects, diagnosis, and treatment of the Kaufman syndrome (hydrocolpos, hypospadias, polydactyly).

Hofmann U, Dopfer R, Reifferscheid P.

Prog Pediatr Surg. 1984;17:71-8.

PMID:
6425984
17.

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.

PMID:
12477087
18.

Weyers acrodental dysostosis in a family.

Roubicek M, Spranger J.

Clin Genet. 1984 Dec;26(6):587-90.

PMID:
6499270
19.

Cryptomicrotia and short, stubby fingers with excess fingertip arch patterns in a mother and son.

Tonoki H, Ohura T, Niikawa N.

Am J Med Genet. 1988 Apr;29(4):857-62.

PMID:
3400730
20.

Polydactyly: report of a large kindred.

Kirkland LR, Russell RO Jr.

South Med J. 1976 Apr;69(4):436-7.

PMID:
1265503
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