一名患有18号染色体短臂缺失的患者（46，XY，18p-）。 - Suppr

A patient with a short arm deletion of chromosome 18 (46,XY,18p-).

作者信息

Weiss L, Mayeda K

出版信息

J Med Genet. 1969 Jun;6(2):216-9. doi: 10.1136/jmg.6.2.216.

DOI:10.1136/jmg.6.2.216

PMID:5801470

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468842/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f539/1468842/61c0771d3e08/jmedgene00373-0107-a.jpg

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Familial Langdon Down anomaly with chromosomal fusion.

Ann Hum Genet. 1961 Dec;25:243-52. doi: 10.1111/j.1469-1809.1962.tb01524.x.

FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

Am J Hum Genet. 1965 Sep;17(5):410-9.

PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.

Am J Hum Genet. 1964 Sep;16(3):364-74.

ABO FREQUENCIES IN MONGOLS.

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[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].

C R Hebd Seances Acad Sci. 1963 Nov 18;257:3098-102.

A search for autosomal linkage in a trisomic population: blood group frequencies in Mongols.

Am J Hum Genet. 1962 Dec;14(4):317-34.

Familial mongolism.

Cytogenetics. 1962;1:141-79. doi: 10.1159/000129726.

Chromosome preparations of leukocytes cultured from human peripheral blood.

Exp Cell Res. 1960 Sep;20:613-6. doi: 10.1016/0014-4827(60)90138-5.

Ring 1 chromosome and dwarfism--a possible syndrome.

J Pediatr. 1967 Nov;71(5):719-22. doi: 10.1016/s0022-3476(67)80211-7.

Deletion of the long arm of chromosome 16 and an unexpected Duffy blood group phenotype reveal a possible autosomal linkage.

Nature. 1967 Sep 2;215(5105):1075-6. doi: 10.1038/2151075a0.

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A patient with a short arm deletion of chromosome 18 (46,XY,18p-).

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