Related Experiment Videos
47,XXY karyotype in a patient with Beckwith-Wiedemann syndrome
Annales De Genetique
|January 1, 1986
Abstract:
The present report summarizes the follow-up data from birth up to the age of 14 years in a male patient with Beckwith-Wiedemann syndrome and 47,XXY karyotype.
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
The Floating-Harbor syndrome: two affected siblings in a family.
Clinical genetics·1996
XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning.
Genetic counseling (Geneva, Switzerland)·1995
Tetrasomy 9p: prenatal diagnosis and fetopathological findings in a second trimester male fetus.
Annales de genetique·1994
Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years).
Genetic counseling (Geneva, Switzerland)·1993
A distinct multiple congenital anomalies syndrome associated with distal 5q deletion (q35.1qter).
Annales de genetique·1993
Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
Genetic counseling (Geneva, Switzerland)·1993
Large duplication 4q25-q34 with mild clinical effect.
Annales de genetique·2004
Partial trisomy 8q and partial monosomy 18p: a case report.
Annales de genetique·2004
Premenstrual Disorders in Adolescents: An Interdisciplinary Perspective.
Journal of clinical medicine·2026
Obesity, Oxidative Stress, and Inflammation in Precocious Puberty: Do All Roads Lead to the Hypothalamus?
International journal of molecular sciences·2026