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Items: 13

1.

Left ventricular noncompaction: a rare disorder in adults and its association with 1p36 chromosomal anomaly.

Dod HS, Bhardwaj R, Hummel M, Morise AP, Batish S, Warden BE, Beto RJ, Jain AC.

Am J Med Genet A. 2010 Jan;152A(1):191-5. doi: 10.1002/ajmg.a.33155.

PMID:
20034097
2.

Left Ventricular Non-compaction: Is It Genetic?

Ting TW, Jamuar SS, Brett MS, Tan ES, Cham BW, Lim JY, Law HY, Tan EC, Choo JT, Lai AH.

Pediatr Cardiol. 2015 Dec;36(8):1565-72. doi: 10.1007/s00246-015-1222-5. Epub 2015 Jun 25. Review.

PMID:
26108892
3.

Left ventricular noncompaction.

Ichida F.

Circ J. 2009 Jan;73(1):19-26. Epub 2008 Dec 4. Review.

4.

Tetrasomy 8 as a primary chromosomal abnormality in a child with acute megakaryoblastic leukemia. a case report and review of the literature.

Aktas D, Tuncbilek E, Cetin M, Hicsonmez G.

Cancer Genet Cytogenet. 2001 Apr 15;126(2):166-8. Review.

PMID:
11376811
5.

Monosomy 1p36 deletion syndrome.

Gajecka M, Mackay KL, Shaffer LG.

Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):346-56. Review.

PMID:
17918734
6.

Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature.

Faivre L, Morichon-Delvallez N, Viot G, Martinovic J, Pinson MP, Aubry JP, Raclin V, Edery P, Dumez Y, Munnich A, Vekemans M.

Prenat Diagn. 1999 Jan;19(1):49-53. Review.

PMID:
10073907
7.

Monosomy 1p36.

Slavotinek A, Shaffer LG, Shapira SK.

J Med Genet. 1999 Sep;36(9):657-63. Review.

8.

Genetic heterogeneity of left-ventricular noncompaction cardiomyopathy.

Moric-Janiszewska E, Markiewicz-Łoskot G.

Clin Cardiol. 2008 May;31(5):201-4. Review.

9.

Interstitial deletion 2(p11.2p13): a rare chromosomal abnormality.

Wenger SL, McPherson EW.

Clin Genet. 1997 Jul;52(1):61-2. Review.

PMID:
9272715
10.

Cytogenetic abnormalities in hepatoblastoma: report of two new cases and review of the literature suggesting imbalance of chromosomal regions on chromosomes 1, 4, and 12.

Nagata T, Nakamura M, Shichino H, Chin M, Sugito K, Ikeda T, Koshinaga T, Fukuzawa M, Inoue M, Mugishima H.

Cancer Genet Cytogenet. 2005 Jan 1;156(1):8-13. Review.

PMID:
15588850
11.

Synovial chondromatosis: clonal chromosome changes provide further evidence for a neoplastic disorder.

Sciot R, Dal Cin P, Bellemans J, Samson I, Van den Berghe H, Van Damme B.

Virchows Arch. 1998 Aug;433(2):189-91. Review.

PMID:
9737798
12.

Left ventricular noncompaction.

Pantazis AA, Elliott PM.

Curr Opin Cardiol. 2009 May;24(3):209-13. doi: 10.1097/HCO.0b013e32832a11e7. Review.

PMID:
19318934
13.

[ICF syndrome. Immunodeficiency, chromosomal centromere instability, facial anomalies. Case report and literature review].

Kieback P, Wendisch H, Lorenz P, Hinkel K.

Monatsschr Kinderheilkd. 1992 Feb;140(2):91-4. Review. German.

PMID:
1557060

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