A 4q21-q22 deletion in a girl with severe growth retardation [1]

Clinical Genetics

Volumn 61, Issue 3, 2002, Pages 226-228

  Harada, N ^b   Nagai, T ^b   Shimokawa, O ^b   Niikawa, N ^b   Matsumoto, N ^a  

^a NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; OSTEOGENIN; PROTEIN DMP1; PROTEIN DSPP; PROTEIN IBSP; PROTEIN MEPE; PROTEIN PRKG2; PROTEIN SNCA; UNCLASSIFIED DRUG;

CASE REPORT; CHROMOSOME 4Q; CHROMOSOME ANALYSIS; CLINICAL FEATURE; DISEASE SEVERITY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENE EXPRESSION; GENE LOSS; GENE MAPPING; GENE MUTATION; GROWTH RETARDATION; HEARING LOSS; HUMAN; HYPERTELORISM; INTERSTITIAL CHROMOSOME DELETION; LETTER; PATHOGENESIS; PRESCHOOL CHILD; PRIORITY JOURNAL; SHORT STATURE; SKULL MALFORMATION; TOOTH DISEASE;

CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; GROWTH DISORDERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING;

EID: 0036524266     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2002.610311.x     Document Type: Letter

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