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Results: 1 to 20 of 144

Similar articles for PubMed (Select 14518066)

1.

Feingold syndrome: clinical review and genetic mapping.

Celli J, van Bokhoven H, Brunner HG.

Am J Med Genet A. 2003 Nov 1;122A(4):294-300. Review.

PMID:
14518066
2.

[Feingold syndrome].

Alessandri JL, Graber D, Tiran-Rajaofera I, Montbrun A, Pilorget H, Samperiz S, Attali T, de Napoli-Cocci S.

Arch Pediatr. 2000 Jun;7(6):637-40. French.

PMID:
10911531
3.

A Feingold syndrome case with previously undescribed features and a new mutation.

Koçak H, Ozaydin E, Köse G, Marcelis CL, Kamsteeg EJ, Ceylaner S.

Genet Couns. 2009;20(3):261-7.

PMID:
19852433
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.

Digital anomalies, microcephaly, and normal intelligence: new syndrome or Feingold syndrome?

Kawame H, Pagon RA, Hudgins L.

Am J Med Genet. 1997 Mar 31;69(3):240-4.

PMID:
9096751
6.

Feingold syndome: a rare but important cause of syndromic tracheoesophageal fistula.

Layman-Pleet L, Jackson CC, Chou S, Boycott KM.

J Pediatr Surg. 2007 Sep;42(9):E1-3.

PMID:
17848225
7.

Imperforate anus in Feingold syndrome.

Büttiker V, Wojtulewicz J, Wilson M.

Am J Med Genet. 2000 May 29;92(3):166-9.

PMID:
10817649
8.

Familial syndromic esophageal atresia maps to 2p23-p24.

Celli J, van Beusekom E, Hennekam RC, Gallardo ME, Smeets DF, de Córdoba SR, Innis JW, Frydman M, König R, Kingston H, Tolmie J, Govaerts LC, van Bokhoven H, Brunner HG.

Am J Hum Genet. 2000 Feb;66(2):436-44.

10.

A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome.

Chen CP, Lin SP, Chern SR, Wu PS, Chang SD, Ng SH, Liu YP, Su JW, Wang W.

Eur J Med Genet. 2012 Nov;55(11):666-9. doi: 10.1016/j.ejmg.2012.07.003. Epub 2012 Jul 25.

PMID:
22842076
11.

Genotype-phenotype correlations in MYCN-related Feingold syndrome.

Marcelis CL, Hol FA, Graham GE, Rieu PN, Kellermayer R, Meijer RP, Lugtenberg D, Scheffer H, van Bokhoven H, Brunner HG, de Brouwer AP.

Hum Mutat. 2008 Sep;29(9):1125-32. doi: 10.1002/humu.20750.

PMID:
18470948
13.

Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies.

Innis JW, Asher JH Jr, Poznanski AK, Sheldon S.

Am J Med Genet. 1997 Aug 8;71(2):150-5.

PMID:
9217213
14.

Vertebral defects in a patient with Feingold syndrome.

Kellermayer R, Weisenbach J, Gyuris P, Aszmann M, Kosztolányi G.

Clin Dysmorphol. 2005 Oct;14(4):213-4. No abstract available.

PMID:
16155427
15.

Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.

Svensson AM, Curry CJ, South ST, Whitby H, Maxwell TM, Aston E, Fisher J, Carmack CE, Scheffer A, Abu-Shamsieh A, Brothman AR.

Am J Med Genet A. 2007 Jun 15;143A(12):1348-53.

PMID:
17506097
16.

Okihiro syndrome is caused by SALL4 mutations.

Kohlhase J, Heinrich M, Schubert L, Liebers M, Kispert A, Laccone F, Turnpenny P, Winter RM, Reardon W.

Hum Mol Genet. 2002 Nov 1;11(23):2979-87.

17.

[Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?].

Shongo MY, Lubala TK, Mbuyi SM, Makinko PI, Ngwej DT, Kabange FN.

Pan Afr Med J. 2012;13:85. Epub 2012 Dec 20. French. No abstract available.

18.

Familial syndromic duodenal atresia: Feingold syndrome.

Holder-Espinasse M, Ahmad Z, Hamill J, Pahari A, Misra D, Drake D, Winter RM, Wilson LC.

Eur J Pediatr Surg. 2004 Apr;14(2):112-6.

PMID:
15185158
19.

Cerebral and cerebellar white matter abnormalities with magnetic resonance imaging in a child with Feingold syndrome.

Lehman VT, Patterson MC, Babovic-Vuksanovic D, Rydberg C.

Am J Med Genet A. 2009 Dec;149A(12):2824-7. doi: 10.1002/ajmg.a.33108.

PMID:
19921653
20.

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
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