Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder.

Dudley, Oenone; Muscatelli, F

Dudley, Oenone; Muscatelli, F.

Affiliation

Dudley O; NMDA, UMR CNRS 6156, Intitut de Biologie Moléculaire de Luminy (IBDML), Campus de Luminy, Case 907, 13288 Marseille, France. odudley@ibdml.univ-mrs.fr

Early Hum Dev ; 83(7): 471-8, 2007 Jul.

Article in En | MEDLINE | ID: mdl-17055193

Subject(s)

Fetal Growth Retardation/etiology; Genomic Imprinting; Prader-Willi Syndrome/complications; Adolescent; Adult; Child; Child, Preschool; Chromosome Aberrations; DNA/analysis; Female; Fetal Growth Retardation/diagnosis; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases/etiology; Male; Middle Aged; Prader-Willi Syndrome/genetics; Pregnancy; Pregnancy Complications

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Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / Genomic Imprinting / Fetal Growth Retardation Type of study: Diagnostic_studies / Etiology_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Language: En Journal: Early Hum Dev Year: 2007 Document type: Article

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