Identifying genes responsible for intellectual disability in consanguineous families

Human Heredity

Volumn 77, Issue 1-4, 2014, Pages 150-160

  Iqbal, Zafar ^a   Van Bokhoven, Hans ^a,b  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY   (Netherlands)

Author keywords

Autosomal recessive intellectual disability; Consanguinity; Exome sequencing; Heterogeneity; Next generation sequencing

Indexed keywords

DNA;

ARTICLE; CONSANGUINEOUS MARRIAGE; CONSANGUINITY; GENE IDENTIFICATION; GENE MAPPING; GENETIC COUNSELING; GENETIC IDENTIFICATION; GENOTYPING TECHNIQUE; HOMOZYGOSITY; HUMAN; INTELLECTUAL IMPAIRMENT; META ANALYSIS (TOPIC); MONOGENIC DISORDER; NONHUMAN; PAKISTAN; ANEUPLOIDY; BRAIN DAMAGE; COPY NUMBER VARIATION; FETUS HYPOXIA; GENETIC VARIABILITY; INJURY; LOW BIRTH WEIGHT; NEXT GENERATION SEQUENCING; RECURRENT DISEASE; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; TRISOMY 21; GENETICS; HIGH THROUGHPUT SEQUENCING; HOMOZYGOTE; INTELLECTUAL DISABILITY; PATHOLOGY; PEDIGREE; PREVALENCE; PROCEDURES; RECESSIVE GENE; SOCIOECONOMICS;

ANIMALIA;

CONSANGUINITY; GENES, RECESSIVE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HOMOZYGOTE; HUMANS; INTELLECTUAL DISABILITY; PAKISTAN; PEDIGREE; PREVALENCE; RISK FACTORS; SOCIOECONOMIC FACTORS;

EID: 84904876062     PISSN: 00015652     EISSN: 14230062     Source Type: Journal    
DOI: 10.1159/000360539     Document Type: Article

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