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Items: 1 to 20 of 31

1.

Variation in severity of cardiac disease in Holt-Oram syndrome.

Sletten LJ, Pierpont ME.

Am J Med Genet. 1996 Oct 16;65(2):128-32. Review.

PMID:
8911604
2.

Cardiac malformations associated with the Holt-Oram syndrome--report on a family and review of the literature.

Bossert T, Walther T, Gummert J, Hubald R, Kostelka M, Mohr FW.

Thorac Cardiovasc Surg. 2002 Oct;50(5):312-4. Review.

PMID:
12375192
3.

[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome].

Bonnet D, Terrett J, Pequignot-Viegas E, Weissenbach J, Munnich A, Lyonnet S, Kachaner J.

Arch Mal Coeur Vaiss. 1995 May;88(5):661-6. Review. French.

PMID:
7646274
4.

Pedigree analysis and descriptive investigation of three classic phenotypes associated with Holt-Oram syndrome.

Lehner R, Goharkhay N, Tringler B, Fasching C, Hengstschläger M.

J Reprod Med. 2003 Mar;48(3):153-9. Review.

PMID:
12698771
5.

[Holt-Oram syndrome. Review and report of 2 familial cases].

Oliveira M, Agapito A, Rosário L, Galrinho A, da Silva N, Prates A, Antunes AM.

Rev Port Cardiol. 1994 Dec;13(12):929-32, 893. Review. Portuguese.

PMID:
7873223
6.

[The Holt-Oram syndrome. Review of the literature and current orthopedic treatment concepts].

Weber M, Wenz W, van Riel A, Kaufmann A, Graf J.

Z Orthop Ihre Grenzgeb. 1997 Jul-Aug;135(4):368-75. Review. German.

PMID:
9381776
7.

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
8.

Current advances in Holt-Oram syndrome.

Huang T.

Curr Opin Pediatr. 2002 Dec;14(6):691-5. Review.

PMID:
12436037
9.

[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
10.

Ritscher-Schinzel (3C) syndrome: documentation of the phenotype.

Kosaki K, Curry CJ, Roeder E, Jones KL.

Am J Med Genet. 1997 Feb 11;68(4):421-7. Review.

PMID:
9021015
11.

[Holt-Oram syndrome. Presentation of a clinical case].

Amilachwari M, Capriles MA, Regalado de Amilachwari ME, Zerpa-Caires F.

Bol Med Hosp Infant Mex. 1991 Aug;48(8):570-5. Review. Spanish.

PMID:
1953978
12.

Holt-Oram Syndrome.

McDermott DA, Fong JC, Basson CT.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2004 Jul 20 [updated 2015 Oct 8].

13.

[Cayler's cardio-facial syndrome. Apropos of 19 cases].

Perrin P, Worms AM, Marçon F, Perrin C, Pernot C.

Arch Fr Pediatr. 1989 Apr;46(4):257-61. Review. French.

PMID:
2665683
14.

New understandings in the genetics of congenital heart disease.

Benson DW, Basson CT, MacRae CA.

Curr Opin Pediatr. 1996 Oct;8(5):505-11. Review.

PMID:
8946132
15.

[Extracardiac malformations in infants with congenital heart diseases: clinical research and statistics covering period 1969-79 (author's transl)].

Belisario C, Generoso M, Brandigi L, Menci R, Merello G, Ammanati V.

Pediatr Med Chir. 1981 Sep-Oct;3(5):363-8. Review. Italian.

PMID:
7045823
16.

Genetic counseling in congenital heart disease.

Ardinger RH Jr.

Pediatr Ann. 1997 Feb;26(2):99-104. Review.

PMID:
9121847
17.

Genetics of congenital heart defects: a candidate gene approach.

Lagendijk AK, Smith KA, Bakkers J.

Trends Cardiovasc Med. 2010 May;20(4):124-8. doi: 10.1016/j.tcm.2010.10.003. Review.

PMID:
21335282
18.

Cantrell's syndrome: a challenge to the surgeon.

Vazquez-Jimenez JF, Muehler EG, Daebritz S, Keutel J, Nishigaki K, Huegel W, Messmer BJ.

Ann Thorac Surg. 1998 Apr;65(4):1178-85. Review.

PMID:
9564963
19.

Genetics and congenital heart disease.

Emanuel R.

Br Heart J. 1970 May;32(3):281-91. Review.

20.

Further delineation of the Baller-Gerold syndrome.

Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ.

Am J Med Genet. 1993 Feb 15;45(4):519-24. Review.

PMID:
8465861

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