Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region.

Dieter Kotzot

doi:10.1034/j.1399-0004.2001.600309.x

Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region.

Dieter Kotzot

Institute of Human Genetics

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

9 Citations (Web of Science)

Original language	English
Pages (from-to)	226-231
Journal	CLINICAL GENETICS
Volume	60
Issue number	3
DOIs	https://doi.org/10.1034/j.1399-0004.2001.600309.x
Publication status	Published - 2001

Keywords

INTRAUTERINE GROWTH-RETARDATION
SILVER-RUSSELL-SYNDROME
CHROMOSOME 14Q
PRADER-WILLI
PHENOTYPE
MOSAICISM
KARYOTYPE
PROBANDS
PUBERTY
ORIGIN

Access to Document

10.1034/j.1399-0004.2001.600309.x

Cite this

@article{85202843f3ad436bb804c69266d828c9,

title = "Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region.",

keywords = "INTRAUTERINE GROWTH-RETARDATION, SILVER-RUSSELL-SYNDROME, CHROMOSOME 14Q, PRADER-WILLI, PHENOTYPE, MOSAICISM, KARYOTYPE, PROBANDS, PUBERTY, ORIGIN",

author = "Dieter Kotzot",

year = "2001",

doi = "10.1034/j.1399-0004.2001.600309.x",

language = "English",

volume = "60",

pages = "226--231",

journal = "CLINICAL GENETICS",

issn = "0009-9163",

publisher = "Wiley Verlag ",

number = "3",

}

TY - JOUR

T1 - Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region.

AU - Kotzot, Dieter

PY - 2001

Y1 - 2001

KW - INTRAUTERINE GROWTH-RETARDATION

KW - SILVER-RUSSELL-SYNDROME

KW - CHROMOSOME 14Q

KW - PRADER-WILLI

KW - PHENOTYPE

KW - MOSAICISM

KW - KARYOTYPE

KW - PROBANDS

KW - PUBERTY

KW - ORIGIN

U2 - 10.1034/j.1399-0004.2001.600309.x

DO - 10.1034/j.1399-0004.2001.600309.x

M3 - Original Article

C2 - 11595025

SN - 0009-9163

VL - 60

SP - 226

EP - 231

JO - CLINICAL GENETICS

JF - CLINICAL GENETICS

IS - 3

ER -