Seckel syndrome with chromosomal 18 deletion

Indian Journal of Pediatrics

Volumn 76, Issue 12, 2009, Pages 1270-1271

  Panigrahi, Inusha ^a   Kaur, Satvinder ^a   Kulkarni, Ketan ^a   Das, Reena ^a   Marwaha, Ram Kumar ^a  

^a POSTGRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH   (India)

Author keywords

Chromosome 18; Heterogeneity; Microcephaly; Neuroimaging; Seckel syndrome

Indexed keywords

ARTICLE; BIRTH WEIGHT; BLOOD SAMPLING; BODY HEIGHT; CASE REPORT; CHILD; CHROMOSOME 18; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; DWARFISM; ECHOCARDIOGRAPHY; FEMALE; GIEMSA STAIN; HEAD CIRCUMFERENCE; HEART ATRIUM SEPTUM DEFECT; HUMAN; MALE; MEDICAL RECORD; MICROCEPHALY; NUCLEAR MAGNETIC RESONANCE IMAGING; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PULMONARY HYPERTENSION; SECKEL SYNDROME; T LYMPHOCYTE;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; CRANIOFACIAL ABNORMALITIES; DWARFISM; FEMALE; HUMANS; INFANT; MALE; MENTAL RETARDATION; MICROCEPHALY; SYNDROME;

EID: 76649089953     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12098-009-0223-x     Document Type: Article

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