[artículo] 
inThe American Journal of Psychiatry > Año 2018 - Vol. 175 - No.5 (Mayo) . - pp. 400-407

Título :	Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington’s Disease
Tipo de documento:	texto impreso
Autores:	Martilias Farrell, Autor ; Maya Lichtenstein, Autor ; James J. Crowley, Autor
Fecha de publicación:	2018
Artículo en la página:	pp. 400-407
Idioma :	Inglés (eng) Idioma original : Inglés (eng)
Palabras clave:	Demencia de aparición temprana, Enfermedad de Huntington, 22q11 DS, Genética, Esquizofrenia
Resumen:	This case provides an example of genetic conditions associated with “copy number variation,” where portions of the genome are either excessively repeated as “copies” (i.e., duplications) or where normal “copies” are absent (i.e., deletions). The early-life developmental abnormalities in this patient were associated with what?
Link:	./index.php?lvl=notice_display&id=17319

[artículo] Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington’s Disease [texto impreso] / Martilias Farrell, Autor ; Maya Lichtenstein, Autor ; James J. Crowley, Autor . - 2018 . - pp. 400-407.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in The American Journal of Psychiatry > Año 2018 - Vol. 175 - No.5 (Mayo) . - pp. 400-407

Palabras clave:	Demencia de aparición temprana, Enfermedad de Huntington, 22q11 DS, Genética, Esquizofrenia
Resumen:	This case provides an example of genetic conditions associated with “copy number variation,” where portions of the genome are either excessively repeated as “copies” (i.e., duplications) or where normal “copies” are absent (i.e., deletions). The early-life developmental abnormalities in this patient were associated with what?
Link:	./index.php?lvl=notice_display&id=17319