Two infants with del(3)(p25pter) and a review of previously reported cases

Jeanette Ramer; Roger Ladda; C. Frankel

doi:10.1002/ajmg.1320330115

Two infants with del(3)(p25pter) and a review of previously reported cases

Jeanette Ramer, Roger Ladda, C. Frankel

Research output: Contribution to journal › Review article › peer-review

23 Scopus citations

Abstract

Del(3)(p25pter) is associated with a characteristic multiple congenital anomalies/mental retardation syndrome. Early recognition of these manifestations and identification of the chromosome defect are essential for proper management and counseling.

Original language	English (US)
Pages (from-to)	108-112
Number of pages	5
Journal	American Journal of Medical Genetics
Volume	33
Issue number	1
DOIs	https://doi.org/10.1002/ajmg.1320330115
State	Published - 1989

All Science Journal Classification (ASJC) codes

Genetics(clinical)

Access to Document

10.1002/ajmg.1320330115

Cite this

@article{1de2285dac9a4fbbb7baed8db38dfd53,

title = "Two infants with del(3)(p25pter) and a review of previously reported cases",

abstract = "Del(3)(p25pter) is associated with a characteristic multiple congenital anomalies/mental retardation syndrome. Early recognition of these manifestations and identification of the chromosome defect are essential for proper management and counseling.",

author = "Jeanette Ramer and Roger Ladda and C. Frankel",

year = "1989",

doi = "10.1002/ajmg.1320330115",

language = "English (US)",

volume = "33",

pages = "108--112",

journal = "American Journal of Medical Genetics",

issn = "0148-7299",

publisher = "Wiley-Liss Inc.",

number = "1",

}

TY - JOUR

T1 - Two infants with del(3)(p25pter) and a review of previously reported cases

AU - Ramer, Jeanette

AU - Ladda, Roger

AU - Frankel, C.

PY - 1989

Y1 - 1989

N2 - Del(3)(p25pter) is associated with a characteristic multiple congenital anomalies/mental retardation syndrome. Early recognition of these manifestations and identification of the chromosome defect are essential for proper management and counseling.

AB - Del(3)(p25pter) is associated with a characteristic multiple congenital anomalies/mental retardation syndrome. Early recognition of these manifestations and identification of the chromosome defect are essential for proper management and counseling.

UR - http://www.scopus.com/inward/record.url?scp=0024362209&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0024362209&partnerID=8YFLogxK

U2 - 10.1002/ajmg.1320330115

DO - 10.1002/ajmg.1320330115

M3 - Review article

C2 - 2665488

AN - SCOPUS:0024362209

SN - 0148-7299

VL - 33

SP - 108

EP - 112

JO - American Journal of Medical Genetics

JF - American Journal of Medical Genetics

IS - 1

ER -

Two infants with del(3)(p25pter) and a review of previously reported cases

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this