Variations of heterochromatic chromosomal regions and chromosome abnormalities in children with autism: Identification of genetic markers in autistic spectrum disorders

Zhurnal Nevrologii i Psihiatrii imeni S.S. Korsakova

Volumn 106, Issue 6, 2006, Pages 52-57

  Vorsanova, S G ^a   Jourov, I Yu ^a   Demidova, I A ^a   Voinova Ulas, V Yu ^a   Kravets, V S ^a   Soloviev, I V ^a   Gorbachevskaya, N L ^a   Yurov, Yu B ^a  

^a NONE

Author keywords

Autism; Chromosome abnormalities; Cytogenetic and molecular cytogenetic analysis; Variations of heterochromatic regions

Indexed keywords

DNA;

ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 1; CHROMOSOME 16; CHROMOSOME 9; CHROMOSOME ABERRATION; COMPARATIVE STUDY; FEMALE; FOLLOW UP; GENETIC MARKER; GENETICS; HETEROCHROMATIN; HUMAN; IN SITU HYBRIDIZATION; INFANT; MALE; PRESCHOOL CHILD; PROGNOSIS;

ADOLESCENT; ADULT; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 9; DNA; FEMALE; FOLLOW-UP STUDIES; GENETIC MARKERS; HETEROCHROMATIN; HUMANS; IN SITU HYBRIDIZATION; INFANT; MALE; PROGNOSIS;

EID: 33746803814     PISSN: 19977298     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (21)

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