Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases
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Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases. / Michaelsen, Kim F.; Lundsteen, Claes; Hansen, Flemming Juul.
In: Clinical Genetics, Vol. 16, No. 3, 1979, p. 147-150.Research output: Contribution to journal › Journal article › Research › peer-review
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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