Chromosomal Microarray Study in Prader-Willi Syndrome

A high-resolution chromosome microarray analysis was performed on 154 consecutive individuals enrolled in the DESTINY PWS clinical trial for Prader-Willi syndrome (PWS). Of these 154 PWS individuals, 87 (56.5%) showed the typical 15q11-q13 deletion subtypes, 62 (40.3%) showed non-deletion maternal d...

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Veröffentlicht in:	International journal of molecular sciences 2023-01, Vol.24 (2), p.1220
Hauptverfasser:	Butler, Merlin G, Hossain, Waheeda A, Cowen, Neil, Bhatnagar, Anish
Format:	Artikel
Sprache:	eng
Schlagworte:	Chromosomes Chromosomes, Human, Pair 15 - genetics Cognition & reasoning Family Females Genetic counseling Genetic disorders Genetic testing High resolution Humans Klinefelter's syndrome Male Males Microarray Analysis Prader-Willi syndrome Prader-Willi Syndrome - genetics Self destructive behavior X chromosomes
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