SCOPUS 정보 검색 플랫폼

Nature Genetics

Volumn 46, Issue 10, 2014, Pages 1046-1048

Reaching a CNV milestone

(1) Beaudet, Arthur L a

a BAYLOR COLLEGE OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; AUTISM; BIPOLAR DISORDER; CARRIER TESTING; CLINICAL GENETICS; COGNITIVE DEFECT; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; EARLY INTERVENTION; EPILEPSY; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HUMAN GENOME; HUMAN GENOME PROJECT; INTELLECTUAL IMPAIRMENT; KARYOTYPING; MICROARRAY ANALYSIS; NEWBORN SCREENING; PENETRANCE; PHENOTYPE; PHENOTYPIC VARIATION; POINT MUTATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RADIUS APLASIA; SCHIZOPHRENIA; SHORT SURVEY; THROMBOCYTOPENIA; FEMALE; GENETIC PREDISPOSITION; GENETICS; MALE;

AUTISTIC DISORDER; DEVELOPMENTAL DISABILITIES; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE;

EID: 84922063978 PISSN: 10614036 EISSN: 15461718 Source Type: Journal
DOI: 10.1038/ng.3106 Document Type: Short Survey

Times cited : (12)

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