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Links from PubMed

Items: 19

1.

Brachydactyly-short stature-hypertension (Bilginturan) syndrome: report on two families.

Chitayat D, Grix A, Balfe JW, Abramowicz JS, Garza J, Fong CT, Silver MM, Saller DN Jr, Bresnick GH, Giedion A, Lachman RS, Rimoin DL.

Am J Med Genet. 1997 Dec 19;73(3):279-85.

PMID:
9415685
2.

Karsch-Neugebauer syndrome in two sibs with unaffected parents.

Wong SC, Cobben JM, Hiemstra S, Robinson PH, Heeg M.

Am J Med Genet. 1998 Jan 13;75(2):207-10. Review.

PMID:
9450888
3.

Three-generation dominant transmission of the Silver-Russell syndrome.

Duncan PA, Hall JG, Shapiro LR, Vibert BK.

Am J Med Genet. 1990 Feb;35(2):245-50. Review.

PMID:
2178417
4.

Feingold syndrome: report of a new family and review.

Courtens W, Levi S, Verbelen F, Verloes A, Vamos E.

Am J Med Genet. 1997 Nov 28;73(1):55-60. Review.

PMID:
9375923
5.

The distal arthrogryposes: delineation of new entities--review and nosologic discussion.

Hall JG, Reed SD, Greene G.

Am J Med Genet. 1982 Feb;11(2):185-239. Review.

PMID:
7039311
6.

Brachydactyly C, short stature, and hip dysplasia.

Fitch N, Jequier S, Costom B.

Am J Med Genet. 1979;4(2):157-66. Review.

PMID:
391043
7.

Greig cephalopolysyndactyly syndrome in a large family: a comparison of the clinical signs with those described in the literature.

Ausems MG, Ippel PF, Renardel de Lavalette PA.

Clin Dysmorphol. 1994 Jan;3(1):21-30. Review.

PMID:
8205322
8.

Mendelian hypertension with brachydactyly as a molecular genetic lesson in regulatory physiology.

Luft FC, Toka O, Toka HR, Jordan J, Bahring S.

Am J Physiol Regul Integr Comp Physiol. 2003 Oct;285(4):R709-14. Review.

9.

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
10.

Brachydactyly.

Temtamy SA, Aglan MS.

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

11.

Trichorhinophalangeal syndrome type III.

Itin PH, Bohn S, Mathys D, Guggenheim R, Richard G.

Dermatology. 1996;193(4):349-52. Review.

PMID:
8993967
12.

Cooks syndrome: a case report and brief review.

Brennan CB, Buehler T, Lesher JL Jr.

Pediatr Dermatol. 2013 Jul-Aug;30(4):e52-3. doi: 10.1111/j.1525-1470.2011.01668.x. Epub 2012 Feb 13. Review.

PMID:
22329539
14.

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.

15.

Growth deficiency in oculodigitoesophagoduodenal (Feingold) syndrome--case report and review of the literature.

Shaw-Smith C, Willatt L, Thalange N.

Clin Dysmorphol. 2005 Jul;14(3):155-8. Review.

PMID:
15930908
16.

Oligodontia, short stature and small head circumference with normal intelligence.

Melamed Y, Katznelson MB, Frydman M.

Clin Genet. 1994 Oct;46(4):316-8. Review.

PMID:
7834899
17.

Acrodysostosis: report of a 13-year-old boy with review of literature and metacarpophalangeal pattern profile analysis.

Butler MG, Rames LJ, Wadlington WB.

Am J Med Genet. 1988 Aug;30(4):971-80. Review.

PMID:
3055990
18.

Brachydactyly E: isolated or as a feature of a syndrome.

Pereda A, Garin I, Garcia-Barcina M, Gener B, Beristain E, IbaƱez AM, Perez de Nanclares G.

Orphanet J Rare Dis. 2013 Sep 12;8:141. doi: 10.1186/1750-1172-8-141. Review.

19.

[Hypertension with brachydactyly].

Hashimoto T, Ishigami T, Umemura S.

Nihon Rinsho. 2000 Feb;58 Suppl 2:679-83. Review. Japanese. No abstract available.

PMID:
11028427
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