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Items: 1 to 20 of 371

1.

Holt-Oram syndrome: is there a "face"?

Allanson JE, Newbury-Ecob RA.

Am J Med Genet A. 2003 May 1;118A(4):314-8.

PMID:
12687661
2.

Holt-Oram syndrome: a clinical genetic study.

Newbury-Ecob RA, Leanage R, Raeburn JA, Young ID.

J Med Genet. 1996 Apr;33(4):300-7.

3.

The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)

Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, Seidman JG, Seidman CE.

N Engl J Med. 1994 Mar 31;330(13):885-91. Erratum in: N Engl J Med 1994 Jun 2;330(22):1627.

4.

Novel TBX5 mutations in patients with Holt-Oram syndrome.

Debeer P, Race V, Gewillig M, Devriendt K, Frijns JP.

Clin Orthop Relat Res. 2007 Sep;462:20-6.

PMID:
17534187
5.

The face of Smith-Magenis syndrome: a subjective and objective study.

Allanson JE, Greenberg F, Smith AC.

J Med Genet. 1999 May;36(5):394-7.

6.

Holt-Oram syndrome in four half-siblings with unaffected parents: brief clinical report.

Braulke I, Herzog S, Thies U, Zoll B.

Clin Genet. 1991 Apr;39(4):241-4.

PMID:
2070544
7.

[The Holt-Oram syndrome. Entelechy or clinical entity? A mild form of familial presentation].

Palma Nieto JC, Herráez García J, Sciaccaluga Morelli C, Briones García JL.

Rev Esp Cardiol. 1993 Jun;46(6):385-8. Review. Spanish.

PMID:
8316706
8.

Holt-Oram syndrome revisited. Two patients in the same family.

Frota Filho JD, Pereira W, Leiria TL, Vallenas M, Leães PE, Blacher C, Lúcio E, Lucchese FA.

Arq Bras Cardiol. 1999 Nov;73(5):429-34.

9.

Holt-Oram syndrome presenting as agenesis of the left pericardium.

Dias RR, Albuquerque JM, Pereira AC, Stolf NA, Krieger JE, Mady C, Oliveira SA.

Int J Cardiol. 2007 Jan 2;114(1):98-100. Epub 2006 Jan 10.

PMID:
16376438
10.

Genetic heterogeneity of heart-hand syndromes.

Basson CT, Solomon SD, Weissman B, MacRae CA, Poznanski AK, Prieto F, Ruiz de la Fuente S, Pease WE, Levin SE, Holmes LB, et al.

Circulation. 1995 Mar 1;91(5):1326-9.

11.

An operated case of Holt-Oram syndrome with autosomal dominant inheritance.

Czakó Z, Gömöry A, Homolay P, Bacsa S, Kiss S, Móricz F, Fülöp F, Papp Z.

Basic Res Cardiol. 1976 Jan-Feb;71(1):60-7.

PMID:
1259686
12.

Variable clinical expression of Holt-Oram syndrome in three generations.

Oğur G, Gül D, Lenk MK, Imirzalioğlu N, Alpay F, Oğur E.

Turk J Pediatr. 1998 Oct-Dec;40(4):613-8.

PMID:
10028874
13.

Upper-limb-cardiovascular syndrome. Two cases of Holt-Oram syndrome.

Yanase Y, Ueba Y.

Hand. 1978 Feb;10(1):56-60.

PMID:
710983
14.

[Report of a family with Holt-Oram syndrome (author's transl)].

Gaul G, Titscher G, Brand O, Heeger H.

Z Kardiol. 1979 Mar;68(3):173-5. German.

PMID:
442759
15.

Molecular characterization of a 14q deletion in a boy with features of Holt-Oram syndrome.

Le Meur N, Goldenberg A, Michel-Adde C, Drouin-Garraud V, Blaysat G, Marret S, Amara SA, Moirot H, Joly-Hélas G, Mace B, Kleinfinger P, Saugier-Veber P, Frébourg T, Rossi A.

Am J Med Genet A. 2005 May 1;134(4):439-42.

PMID:
15810003
16.

TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed.

Mori AD, Bruneau BG.

Curr Opin Cardiol. 2004 May;19(3):211-5. Review.

PMID:
15096952
17.

The upper limb-cardiovascular syndrome, (Holt-Oram syndrome).

Letts RM, Chudley AE, Cumming G, Shokier MH.

Clin Orthop Relat Res. 1976 May;(116):149-54.

PMID:
1277635
18.

Holt-Oram syndrome.

Lichiardopol C, Militaru C, Popescu B, Hila G, Mixich F.

Rom J Morphol Embryol. 2007;48(1):67-70.

19.

[Holt-Oram syndrome associated with facial anomalies. A case report].

Aviña-Fierro JA, Colonnelli-Barba G.

Rev Med Inst Mex Seguro Soc. 2010 Nov-Dec;48(6):657-9. Spanish.

PMID:
21184723
20.

Heart-hand syndrome.

Saura D, Campos JV, Villegas M, Picó F, de la Morena G, Valdés-Chávarri M.

Int J Cardiol. 2008 Sep 16;129(1):e7-9. Epub 2007 Aug 17.

PMID:
17707532
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