Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray

Molecular Cytogenetics

Volumn 6, Issue 1, 2013, Pages

  Fan, Yao Shan ^a   Ouyang, Xiaomei ^a   Peng, Jinghong ^a   Sacharow, Stephanie ^a   Tekin, Mustafa ^a   Barbouth, Deborah ^a   Bodamer, Olaf ^a   Yusupov, Roman ^b   Navarrete, Christina ^c   Heller, Ana H ^c   Pena, Sérgio Dj ^d  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^b Memorial Regional Hospitals   (United States)

^c JACKSON MEMORIAL HOSPITAL   (United States)

^d Jackson Memorial Hospital ^*  (Brazil)

Author keywords

Chromosome microarray; Consanguinity; Developmental disabilities

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTISM; AUTOSOMAL RECESSIVE DISORDER; BIRTH DEFECT; CHILD; CHROMOSOME ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; CONSANGUINEOUS MARRIAGE; CONSANGUINITY; COPY NUMBER VARIATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; FEMALE; GENETIC COUNSELING; GENETIC RISK; HEREDITY; HOMOZYGOSITY; HUMAN; INBREEDING; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; MICROARRAY ANALYSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; UNIPARENTAL DISOMY;

EID: 84884342502     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-6-38     Document Type: Article

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