A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.

BMC medical genetics

Volumn 11, Issue , 2010, Pages 135-

  Abu Amero, Khaled K ^a   Hellani, Ali M ^b   Salih, Mustafa A ^b   Seidahmed, Mohammad Z ^b   Elmalik, Tageldin S ^b   Zidan, Ghassan ^b   Bosley, Thomas M ^b  

^a KING SAUD UNIVERSITY   (Saudi Arabia)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; AUTISM; CASE REPORT; CHILD; CHROMOSOME 9; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENETIC ASSOCIATION; GENETIC MARKER; GENETICS; HUMAN; INFANT; KARYOTYPING; MALE; NEWBORN; PEDIGREE; PREGNANCY; PRESCHOOL CHILD; SYNDROME;

ADOLESCENT; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 9; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC MARKERS; HUMANS; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; PEDIGREE; PREGNANCY; SYNDROME;

MLCS; MLOWN;

EID: 77956671613     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-11-135     Document Type: Article

References (0)