A case of Williams syndrome with a large, visible cytogenetic deletion [2]

Journal of Medical Genetics

Volumn 36, Issue 12, 1999, Pages 928-932

  Wu, Y Q ^a   Nickerson, E ^a   Shaffer, L G ^a   Keppler Noreuil, K ^a   Muilenburg, A ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AORTA STENOSIS; CASE REPORT; CENTROMERE; CHILD DEVELOPMENT; CHROMOSOME 7Q; CHROMOSOME DELETION; COSMID; DEVELOPMENTAL DISORDER; EXON; FACE DYSMORPHIA; FEMALE; HEMIZYGOSITY; HUMAN; LETTER; MACROCEPHALY; MUSCLE HYPOTONIA; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN HEMANGIOMA; WILLIAMS BEUREN SYNDROME;

CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; FEMALE; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; HUMANS; INFANT; KARYOTYPING; MALE; WILLIAMS SYNDROME;

EID: 0033458057     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (33)