De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes [3]

Journal of Medical Genetics

Volumn 38, Issue 9, 2001, Pages 617-621

  Tonnies H ^a   Schulze, I ^a   Hennies, H C ^a   Neumann, L M ^a   Keitzer, R ^a   Neitzel, H ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; SOMATOMEDIN C; SOMATOMEDIN C RECEPTOR;

CASE REPORT; CHROMOSOME 15Q; CHROMOSOME DELETION; CHROMOSOME PAINTING; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MAPPING; GENE SEQUENCE; GENOME; HUMAN; INFANT; KARYOTYPE; LETTER; LYMPHOCYTE; MOLECULAR GENETICS; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 15; DNA PROBES; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; MICROSATELLITE REPEATS; NUCLEIC ACID HYBRIDIZATION; RECEPTOR, IGF TYPE 1; SENSITIVITY AND SPECIFICITY;

EID: 0034840314     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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