Duplication 14(q24.3q31) in a Father and daughter: Delineation of a possible imprinted region

American Journal of Medical Genetics

Volumn 71, Issue 3, 1997, Pages 361-365

  Robin, N H ^a   Harari Shacham, A ^a   Schwartz, S ^a   Wolff, D J ^a  

^a Center for Human Genetics   (United States)

Author keywords

Chromosome 14q duplication; Imprinting

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 14Q; FEMALE; GENE DOSAGE; GENE DUPLICATION; GENOME IMPRINTING; HUMAN; HUMAN CELL; HUMAN TISSUE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SILENT GENE; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ADULT; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 14; DEVELOPMENTAL DISABILITIES; FACE; FEMALE; GENOMIC IMPRINTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MICROCEPHALY; PHENOTYPE;

EID: 0030746479     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970822)71:3<361::AID-AJMG20>3.0.CO;2-H     Document Type: Article

References (36)