156例先天性心脏病患者的染色体研究。 - Suppr

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Chromosome studies in 156 patients with congenital heart disease.

作者信息

Anders J M, Moores E C, Emanuel R

出版信息

Br Heart J. 1965 Sep;27(5):756-62. doi: 10.1136/hrt.27.5.756.

DOI:10.1136/hrt.27.5.756

PMID:5829760

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC469786/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50da/469786/7fa670acee48/brheartj00340-0133-a.jpg

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Cardiac malformation in mongolism: a prospective study of 184 mongoloid children.

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Ann Hum Genet. 1964 Jun;27:353-65. doi: 10.1111/j.1469-1809.1963.tb01532.x.

CARDIOVASCULAR MALFORMATION IN TURNER'S SYNDROME.

Pediatrics. 1964 Jun;33:919-25.

CHROMOSOME STUDIES IN PATIENTS WITH SUPRAVALVULAR AORTIC STENOSIS.

Lancet. 1963 Aug 31;2(7305):438. doi: 10.1016/s0140-6736(63)92177-9.

AN ABERRANT AUTOSOME (13-15) IN A HUMAN FEMALE AND HER FATHER, BOTH APPARENTLY NORMAL.

Cytogenetics. 1963;2:34-41. doi: 10.1159/000129763.

Chromosomal abnormalities and their relation to disease.

Can Med Assoc J. 1963 Mar 2;88(9):456-61.

Supravalvular aortic stenosis.

Circulation. 1961 Dec;24:1311-8. doi: 10.1161/01.cir.24.6.1311.

Observations on the pathology of the trisomy 17-18 syndrome.

J Pediatr. 1963 May;62:703-9. doi: 10.1016/s0022-3476(63)80040-2.

The D-I trisomy syndrome.

J Pediatr. 1963 Mar;62:326-41. doi: 10.1016/s0022-3476(63)80129-8.

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