一名患有先天性异常的婴儿存在间质性缺失(6)(q11----q15)。 - Suppr

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超能文献

Interstitial deletion (6) (q11----q15) in an infant with congenital abnormalities.

作者信息

Slater H R, Robb A, Forsyth L A, Hamilton D A, Clark M C, Galloway C A

机构信息

Department of Pathology, Raigmore Hospital, Inverness.

出版信息

J Med Genet. 1988 Mar;25(3):210-1. doi: 10.1136/jmg.25.3.210.

DOI:10.1136/jmg.25.3.210

PMID:3351912

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1015492/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4b1/1015492/3276efdf3371/jmedgene00065-0066-a.jpg

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引用本文的文献

Proximal Deletion of 6q Overlapping with Toriello-Carey Facial Phenotype: Prenatal Findings, Clinical Course, Differential Diagnosis, and Review.与托列洛-凯里面部表型重叠的6q近端缺失：产前检查结果、临床病程、鉴别诊断及文献综述

Mol Syndromol. 2017 Dec;9(1):15-21. doi: 10.1159/000484427. Epub 2017 Nov 29.

本文引用的文献

Interstitial deletion of the long arm of chromosome 6 [del(6) (q16q22)]: case report and review of the literature.6号染色体长臂间质缺失[del(6)(q16q22)]：病例报告及文献复习

Clin Genet. 1984 Dec;26(6):574-8. doi: 10.1111/j.1399-0004.1984.tb01106.x.

Deletions of the long arm of chromosome 6: two new cases and review of the literature.6号染色体长臂缺失：两例新病例及文献综述

Am J Med Genet. 1985 Jan;20(1):21-9. doi: 10.1002/ajmg.1320200105.

Congenital anomalies including the VATER association in a patient with del(6)q deletion.一名患有6号染色体长臂缺失的患者出现先天性异常，包括VATER综合征。

J Pediatr. 1977 Dec;91(6):957-60. doi: 10.1016/s0022-3476(77)80903-7.

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