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Items: 1 to 20 of 87

1.

Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients.

Elliott AM, Evans JA.

Am J Med Genet A. 2006 Jul 1;140(13):1419-27.

PMID:
16688749
2.

Pathogenesis of split-hand/split-foot malformation.

Duijf PH, van Bokhoven H, Brunner HG.

Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R51-60. Review.

3.

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.

4.

Split-hand/foot malformation - molecular cause and implications in genetic counseling.

SowiƄska-Seidler A, Socha M, Jamsheer A.

J Appl Genet. 2014 Feb;55(1):105-15. doi: 10.1007/s13353-013-0178-5. Epub 2013 Oct 27. Review.

5.

The expanding panorama of split hand foot malformation.

Basel D, Kilpatrick MW, Tsipouras P.

Am J Med Genet A. 2006 Jul 1;140(13):1359-65. Review.

PMID:
16763964
6.

Split hand foot malformation (SHFM).

Elliott AM, Evans JA, Chudley AE.

Clin Genet. 2005 Dec;68(6):501-5. Review.

PMID:
16283879
7.

Central ray deficiency with extensive syndactyly: a dilemma for classification.

Elliott AM, Reed MH, Evans JA.

Genet Couns. 2009;20(1):27-43. Review.

PMID:
19400540
8.

Clinical, genetic, and molecular aspects of split-hand/foot malformation: an update.

Gurrieri F, Everman DB.

Am J Med Genet A. 2013 Nov;161A(11):2860-72. doi: 10.1002/ajmg.a.36239. Epub 2013 Sep 24. Review.

PMID:
24115638
9.

P63 gene mutations and human developmental syndromes.

Brunner HG, Hamel BC, Bokhoven Hv Hv.

Am J Med Genet. 2002 Oct 15;112(3):284-90. Review.

PMID:
12357472
10.

On the inheritance of the split hand/split foot malformation.

Zlotogora J.

Am J Med Genet. 1994 Oct 15;53(1):29-32. Review.

PMID:
7802032
11.

EEC syndrome: report on 20 new patients, clinical and genetic considerations.

Rodini ES, Richieri-Costa A.

Am J Med Genet. 1990 Sep;37(1):42-53. Review.

PMID:
2240042
12.

Genetics of congenital hand anomalies.

Schwabe GC, Mundlos S.

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

PMID:
15162306
13.

Distal limb malformations: underlying mechanisms and clinical associations.

Sifakis S, Basel D, Ianakiev P, Kilpatrick M, Tsipouras P.

Clin Genet. 2001 Sep;60(3):165-72. Review.

PMID:
11595015
14.

Ectrodactyly and proximal/intermediate interstitial deletion 7q.

McElveen C, Carvajal MV, Moscatello D, Towner J, Lacassie Y.

Am J Med Genet. 1995 Mar 13;56(1):1-5. Review.

PMID:
7747769
15.

Human HOX gene mutations.

Goodman FR, Scambler PJ.

Clin Genet. 2001 Jan;59(1):1-11. Review.

PMID:
11206481
16.

A novel syndrome with psychiatric features and review of malformation syndromes with psychiatric disorders.

du Souich C, Austin JC, Friedlander R, Boerkoel CF.

Am J Med Genet A. 2009 Feb 15;149A(4):713-21. doi: 10.1002/ajmg.a.32709. Review.

PMID:
19253384
18.

Acro-cardio-facial syndrome.

Digilio MC, Dallapiccola B.

Orphanet J Rare Dis. 2010 Sep 29;5:25. doi: 10.1186/1750-1172-5-25. Review.

19.

p63-associated disorders.

Rinne T, Brunner HG, van Bokhoven H.

Cell Cycle. 2007 Feb 1;6(3):262-8. Epub 2007 Feb 3. Review.

PMID:
17224651
20.

Cleft hand/foot: clinical and developmental aspects.

Buss PW.

J Med Genet. 1994 Sep;31(9):726-30. Review.

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