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[Unusual mechanism in Prader-Willi syndrome: incidence in genetic counseling].

Authors :
Klosowski S
Delobel B
Morisot C
Kongolo G
Biancalana V
Thelliez P
Djebara A
Croquette MF
Deroubaix P
Source :
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [Arch Pediatr] 1998 Aug; Vol. 5 (8), pp. 934-5.
Publication Year :
1998

Subjects

Subjects :
Fatal Outcome
Female
Humans
Infant
Infant, Newborn
Karyotyping
Male
Prader-Willi Syndrome diagnosis
Pregnancy
Prenatal Diagnosis
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 9
Genetic Counseling
Prader-Willi Syndrome genetics
Translocation, Genetic genetics

Details

Language :
French
ISSN :
0929-693X
Volume :
5
Issue :
8
Database :
MEDLINE
Journal :
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Publication Type :
Report
Accession number :
9759307
Full Text :
https://doi.org/10.1016/s0929-693x(98)80208-x
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