De novo copy number variants associated with intellectual disability have a paternal origin and age bias

Journal of Medical Genetics

Volumn 48, Issue 11, 2011, Pages 776-778

  Hehir Kwa, Jayne Y ^a   Rodríguez Santiago, Benjamín ^a,b   Vissers, Lisenka E ^a   de Leeuw, Nicole ^a   Pfundt, Rolph ^a   Buitelaar, Jan K ^c   Pérez Jurado, Luis A ^b   Veltman, Joris A ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITAT POMPEU FABRA   (Spain)

^c RADBOUD UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CONTROLLED STUDY; COPY NUMBER VARIATION; ENVIRONMENTAL FACTOR; FEMALE; GENE MUTATION; GENE REARRANGEMENT; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; PATERNAL AGE; PRIORITY JOURNAL; SEGMENTAL DUPLICATION; SINGLE NUCLEOTIDE POLYMORPHISM; SPERMATOGENESIS;

ADULT; ALLELES; COHORT STUDIES; DNA COPY NUMBER VARIATIONS; GENE DOSAGE; HUMANS; INTELLECTUAL DISABILITY; MALE; NETHERLANDS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PATERNAL AGE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEGMENTAL DUPLICATIONS, GENOMIC; SEX FACTORS; SPERMATOGENESIS;

EID: 81055157730     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmedgenet-2011-100147     Document Type: Article

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