Case report: partial trisomy 20q (20q13.13→qter)

Christina M. Sax; Joann N. Bodurtha; Judith A. Brown

doi:10.1111/j.1399-0004.1986.tb01911.x

Case report: partial trisomy 20q (20q13.13→qter)

Christina M. Sax, Joann N. Bodurtha, Judith A. Brown

Research output: Contribution to journal › Article › peer-review

20 Scopus citations

Abstract

Presented here is an infant displaying trisomy of the region 20ql3.13→qter. This case shares phenotypic features with previously reported trisomy 20q individuals.

Original language	English (US)
Pages (from-to)	462-465
Number of pages	4
Journal	Clinical Genetics
Volume	30
Issue number	6
DOIs	https://doi.org/10.1111/j.1399-0004.1986.tb01911.x
State	Published - Dec 1986
Externally published	Yes

Keywords

Chin dimple
congenital heart defect
trisomy 20q

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1111/j.1399-0004.1986.tb01911.x

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title = "Case report: partial trisomy 20q (20q13.13→qter)",

abstract = "Presented here is an infant displaying trisomy of the region 20ql3.13→qter. This case shares phenotypic features with previously reported trisomy 20q individuals.",

keywords = "Chin dimple, congenital heart defect, trisomy 20q",

author = "Sax, {Christina M.} and Bodurtha, {Joann N.} and Brown, {Judith A.}",

year = "1986",

month = dec,

doi = "10.1111/j.1399-0004.1986.tb01911.x",

language = "English (US)",

volume = "30",

pages = "462--465",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell",

number = "6",

}

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T1 - Case report

T2 - partial trisomy 20q (20q13.13→qter)

AU - Sax, Christina M.

AU - Bodurtha, Joann N.

AU - Brown, Judith A.

PY - 1986/12

Y1 - 1986/12

N2 - Presented here is an infant displaying trisomy of the region 20ql3.13→qter. This case shares phenotypic features with previously reported trisomy 20q individuals.

AB - Presented here is an infant displaying trisomy of the region 20ql3.13→qter. This case shares phenotypic features with previously reported trisomy 20q individuals.

KW - Chin dimple

KW - congenital heart defect

KW - trisomy 20q

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U2 - 10.1111/j.1399-0004.1986.tb01911.x

DO - 10.1111/j.1399-0004.1986.tb01911.x

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AN - SCOPUS:0022975156

SN - 0009-9163

VL - 30

SP - 462

EP - 465

JO - Clinical Genetics

JF - Clinical Genetics

IS - 6

ER -

Case report: partial trisomy 20q (20q13.13→qter)

Abstract

Keywords

ASJC Scopus subject areas

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