Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Standard

Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases. / Michaelsen, Kim F.; Lundsteen, Claes; Hansen, Flemming Juul.

I: Clinical Genetics, Bind 16, Nr. 3, 1979, s. 147-150.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Michaelsen, KF, Lundsteen, C & Hansen, FJ 1979, 'Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases', Clinical Genetics, bind 16, nr. 3, s. 147-150. https://doi.org/10.1111/j.1399-0004.1979.tb00983.x

APA

Michaelsen, K. F., Lundsteen, C., & Hansen, F. J. (1979). Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases. Clinical Genetics, 16(3), 147-150. https://doi.org/10.1111/j.1399-0004.1979.tb00983.x

Vancouver

Michaelsen KF, Lundsteen C, Hansen FJ. Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases. Clinical Genetics. 1979;16(3):147-150. https://doi.org/10.1111/j.1399-0004.1979.tb00983.x

Author

Michaelsen, Kim F. ; Lundsteen, Claes ; Hansen, Flemming Juul. / Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases. I: Clinical Genetics. 1979 ; Bind 16, Nr. 3. s. 147-150.

Bibtex

@article{218fdd35c7d846289f5ee02afda42015,
title = "Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases",
abstract = "Two cases of the Prader-Willi syndrome with 46, XY/47, XY, + mar are reported. The majority of Prader-Willi patients with chromosome abnormalities have either 15/15 translocations or mosaicism. Both of these aberrations presumably occur after fertilization. A possible relationship between high parental age and chromosome abnormalities in the Prader-Willi syndrome is discussed.",
author = "Michaelsen, {Kim F.} and Claes Lundsteen and Hansen, {Flemming Juul}",
year = "1979",
doi = "10.1111/j.1399-0004.1979.tb00983.x",
language = "English",
volume = "16",
pages = "147--150",
journal = "Clinical Genetics",
issn = "0009-9163",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases

AU - Michaelsen, Kim F.

AU - Lundsteen, Claes

AU - Hansen, Flemming Juul

PY - 1979

Y1 - 1979

N2 - Two cases of the Prader-Willi syndrome with 46, XY/47, XY, + mar are reported. The majority of Prader-Willi patients with chromosome abnormalities have either 15/15 translocations or mosaicism. Both of these aberrations presumably occur after fertilization. A possible relationship between high parental age and chromosome abnormalities in the Prader-Willi syndrome is discussed.

AB - Two cases of the Prader-Willi syndrome with 46, XY/47, XY, + mar are reported. The majority of Prader-Willi patients with chromosome abnormalities have either 15/15 translocations or mosaicism. Both of these aberrations presumably occur after fertilization. A possible relationship between high parental age and chromosome abnormalities in the Prader-Willi syndrome is discussed.

UR - http://www.scopus.com/inward/record.url?scp=0018291022&partnerID=8YFLogxK

U2 - 10.1111/j.1399-0004.1979.tb00983.x

DO - 10.1111/j.1399-0004.1979.tb00983.x

M3 - Journal article

C2 - 573673

AN - SCOPUS:0018291022

VL - 16

SP - 147

EP - 150

JO - Clinical Genetics

JF - Clinical Genetics

SN - 0009-9163

IS - 3

ER -

ID: 258037437