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Volumn 167, Issue 9, 2015, Pages 2098-2102

Deletion of 15q11.2(BP1-BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population

Author keywords

15q11.2; Array CGH; Autism; Developmental delay; Epilepsy; Microdeletion

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; ATTENTION DEFICIT DISORDER; BONE DISEASE; CHILD; CLEFT PALATE; CLINICAL ARTICLE; CLINICAL FEATURE; COPY NUMBER VARIATION; DEVELOPMENTAL DISORDER; EYE DISEASE; FACE DYSMORPHIA; FEEDING DIFFICULTY; FEMALE; GENE DELETION; GENETIC COUNSELING; GENETIC VARIABILITY; HEART DISEASE; HUMAN; INHERITANCE; MALE; MICROARRAY ANALYSIS; MICROCEPHALY; MUSCLE HYPOTONIA; NEUROLOGIC DISEASE; NEWBORN; PHENOTYPE; POPULATION GENETICS; PREVALENCE; PRIORITY JOURNAL; PROMOTER REGION; SEIZURE; SHORT STATURE; SPEECH DELAY; CHROMOSOME 15; CHROMOSOME DELETION; GENETICS; INFANT; PRESCHOOL CHILD; SYNDROME; YOUNG ADULT;

EID: 84939472330     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.37134     Document Type: Article
Times cited : (33)

References (19)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.