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Items: 1 to 20 of 26

1.

Severe limb defects in Hypodactyly mice result from the expression of a novel, mutant HOXA13 protein.

Post LC, Margulies EH, Kuo A, Innis JW.

Dev Biol. 2000 Jan 15;217(2):290-300.

2.

Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalli.

Devriendt K, Jaeken J, Matthijs G, Van Esch H, Debeer P, Gewillig M, Fryns JP.

Am J Hum Genet. 1999 Jul;65(1):249-51. No abstract available.

3.

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.

Brown SA, Warburton D, Brown LY, Yu CY, Roeder ER, Stengel-Rutkowski S, Hennekam RC, Muenke M.

Nat Genet. 1998 Oct;20(2):180-3.

PMID:
9771712
4.

Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.

Goodman F, Giovannucci-Uzielli ML, Hall C, Reardon W, Winter R, Scambler P.

Am J Hum Genet. 1998 Oct;63(4):992-1000.

5.

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract.

Goodman FR, Mundlos S, Muragaki Y, Donnai D, Giovannucci-Uzielli ML, Lapi E, Majewski F, McGaughran J, McKeown C, Reardon W, Upton J, Winter RM, Olsen BR, Scambler PJ.

Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7458-63.

6.

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.

Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, Lindhout D, Cole WG, Henn W, Knoll JH, Owen MJ, Mertelsmann R, Zabel BU, Olsen BR.

Cell. 1997 May 30;89(5):773-9.

7.

Mutation of HOXA13 in hand-foot-genital syndrome.

Mortlock DP, Innis JW.

Nat Genet. 1997 Feb;15(2):179-80.

PMID:
9020844
8.

Polyalanine expansion in synpolydactyly might result from unequal crossing-over of HOXD13.

Warren ST.

Science. 1997 Jan 17;275(5298):408-9. No abstract available.

9.

Synpolydactyly in mice with a targeted deficiency in the HoxD complex.

Zákány J, Duboule D.

Nature. 1996 Nov 7;384(6604):69-71.

PMID:
8900279
10.

Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopod.

Fromental-Ramain C, Warot X, Messadecq N, LeMeur M, Dollé P, Chambon P.

Development. 1996 Oct;122(10):2997-3011.

11.

Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families.

Akarsu AN, Stoilov I, Yilmaz E, Sayli BS, Sarfarazi M.

Hum Mol Genet. 1996 Jul;5(7):945-52.

PMID:
8817328
12.
13.

Know your neighbors: three phenotypes in null mutants of the myogenic bHLH gene MRF4.

Olson EN, Arnold HH, Rigby PW, Wold BJ.

Cell. 1996 Apr 5;85(1):1-4. Review. No abstract available.

14.

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13.

Muragaki Y, Mundlos S, Upton J, Olsen BR.

Science. 1996 Apr 26;272(5261):548-51.

PMID:
8614804
15.

The hand-foot-genital syndrome: on the variable expression in affected males.

Fryns JP, Vogels A, Decock P, van den Berghe H.

Clin Genet. 1993 May;43(5):232-4.

PMID:
8375102
16.

Homeodomain-DNA recognition.

Gehring WJ, Qian YQ, Billeter M, Furukubo-Tokunaga K, Schier AF, Resendez-Perez D, Affolter M, Otting G, Wüthrich K.

Cell. 1994 Jul 29;78(2):211-23. Review. No abstract available.

PMID:
8044836
17.

Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies.

Verp MS, Simpson JL, Elias S, Carson SA, Sarto GE, Feingold M.

Fertil Steril. 1983 Jul;40(1):80-5.

PMID:
6862042
18.

The hand-food-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract.

Stern AM, Gall JC Jr, Perry BL, Stimson CW, Weitkamp LR, Poznanski AK.

J Pediatr. 1970 Jul;77(1):109-16. No abstract available.

PMID:
5450271
19.

The hand-foot-genital (hand-foot-uterus) syndrome: family report and update.

Halal F.

Am J Med Genet. 1988 Jul;30(3):793-803.

PMID:
3189398
20.

Urinary tract abnormalities in hand-foot-genital syndrome.

Verp MS.

Am J Med Genet. 1989 Apr;32(4):555. No abstract available.

PMID:
2774004

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