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Items: 1 to 20 of 53

1.

Associated anomalies in individuals with polydactyly.

Castilla EE, Lugarinho R, da Graça Dutra M, Salgado LJ.

Am J Med Genet. 1998 Dec 28;80(5):459-65.

PMID:
9880209
2.

Laurin-Sandrow syndrome with additional associated manifestations.

Kantaputra PN.

Am J Med Genet. 2001 Jan 22;98(3):210-5. Review.

PMID:
11169557
3.

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
4.

"Holoprosencephaly-polydactyly" (pseudotrisomy 13) syndrome: expansion of the phenotypic spectrum.

Lurie IW, Wulfsberg EA.

Am J Med Genet. 1993 Sep 1;47(3):405-9. Review.

PMID:
8135289
5.

Mirror image duplication of the hands and feet: report of a sporadic case with multiple congenital anomalies.

Hersh JH, Dela Cruz TV, Pietrantoni M, von Drasek-Ascher G, Turnquest MA, Yacoub OA, Joyce MR.

Am J Med Genet. 1995 Nov 20;59(3):341-5. Review.

PMID:
8599358
6.

Brachyphalangy, polydactyly and tibial aplasia/hypoplasia syndrome (OMIM 609945): case report and review of the literature.

Shafeghati Y, Kahrizi K, Najmabadi H, Kuss AW, Ropers HH, Tzschach A.

Eur J Pediatr. 2010 Dec;169(12):1535-9. doi: 10.1007/s00431-010-1267-7. Epub 2010 Jul 27. Review.

PMID:
20661588
7.

Confirmation of genetic homogeneity of syndactyly type IV and triphalangeal thumb-polysyndactyly syndrome in a Chinese family and review of the literature.

Dai L, Guo H, Meng H, Zhang K, Hu H, Yao H, Bai Y.

Eur J Pediatr. 2013 Nov;172(11):1467-73. doi: 10.1007/s00431-013-2071-y. Epub 2013 Jun 22. Review.

PMID:
23793141
8.

Polydactyly of the foot. Literature review and case presentations.

Galois L, Mainard D, Delagoutte JP.

Acta Orthop Belg. 2002 Oct;68(4):376-80. Review.

PMID:
12415940
9.

Laurin-Sandrow syndrome (mirror hands and feet and nasal defects): description of a new case.

Martínez-Frías ML, Alcaraz M, Espejo P, Gómez MA, García de León R, González Moro L.

J Med Genet. 1994 May;31(5):410-2. Review.

10.

[Genetic background of isolated forms of congenital malformations of the hand].

Jamsheer A.

Med Wieku Rozwoj. 2008 Jul-Sep;12(3):729-37. Review. Polish.

PMID:
19305023
11.

Genetics of congenital hand anomalies.

Schwabe GC, Mundlos S.

Handchir Mikrochir Plast Chir. 2004 Apr-Jun;36(2-3):85-97. Review.

PMID:
15162306
12.

[In utero exposure to benzodiazepine. Is there a risk for anal atresia with lorazepam?].

Bonnot O, Vollset SE, Godet PF, d'Amato T, Dalery J, Robert E.

Encephale. 2003 Nov-Dec;29(6):553-9. Review. French.

PMID:
15029090
13.

Clinical features and teratogenic mechanisms of congenital absence of digits.

Ogino T.

Dev Growth Differ. 2007 Aug;49(6):523-31. Epub 2007 Jun 7. Review.

PMID:
17555519
14.

Brachydactyly.

Temtamy SA, Aglan MS.

Orphanet J Rare Dis. 2008 Jun 13;3:15. doi: 10.1186/1750-1172-3-15. Review.

15.

The p63 gene in EEC and other syndromes.

Brunner HG, Hamel BC, Van Bokhoven H.

J Med Genet. 2002 Jun;39(6):377-81. Review.

16.

Finger polydactyly.

Graham TJ, Ress AM.

Hand Clin. 1998 Feb;14(1):49-64. Review.

PMID:
9526156
17.

Syndactylies and polydactylies: embryological overview and suggested classification.

Winter RM, Tickle C.

Eur J Hum Genet. 1993;1(1):96-104. Review.

PMID:
7915184
18.

[Genetics of congenital hand malformations].

Philip-Sarles N.

Chir Main. 2008 Dec;27 Suppl 1:S7-20. doi: 10.1016/j.main.2008.07.011. Epub 2008 Aug 20. Review. French.

PMID:
18838287
19.

Genetic aspects of polydactyly.

Zguricas J, Heutink P, Heredero L, Deurloo J, Oostra BA, Snijders PJ, Lindhout D, Hovius SE.

Handchir Mikrochir Plast Chir. 1996 Jul;28(4):171-5. Review.

PMID:
8792145
20.

Filippi syndrome: report of three additional cases.

Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA.

Am J Med Genet. 1999 Nov 19;87(2):128-33. Review.

PMID:
10533026

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