De novo terminal deletion of chromosome 7 [46,XX,del(7)(q35)]

Journal of Paediatrics and Child Health

Volumn 32, Issue 4, 1996, Pages 347-349

  Lo, B H ^a,c   Murch, A ^b   Chabros, V ^b   Withnell, R ^a  

^a Disability Services Commission   (Australia)

^b KING EDWARD MEMORIAL HOSPITAL   (Australia)

^c Andrea Way Child Development Centre ^*  (Australia)

Author keywords

Developmental delay; Microcephaly; 46,XX,del(7)(q35)

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 7; CHROMOSOME DELETION; CONDUCTION DEAFNESS; DEVELOPMENTAL DISORDER; FEMALE; GENETICS; GROWTH DISORDER; HUMAN; KARYOTYPING; MICROCEPHALY; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PHENOTYPE;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 7; DEVELOPMENTAL DISABILITIES; FEMALE; GROWTH DISORDERS; HEARING LOSS, CONDUCTIVE; HUMANS; INFANT, NEWBORN; KARYOTYPING; MICROCEPHALY; PHENOTYPE;

EID: 0030208042     PISSN: 10344810     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1440-1754.1996.tb02568.x     Document Type: Article

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