Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH)

Clinical Genetics

Volumn 54, Issue 4, 1998, Pages 334-340

  Benzacken, B ^a   Lapierre, J M ^b   Siffroi, J P ^c   Chalvon, A ^d   Tachdjian, G ^b  

^a HÔPITAL JEAN VERDIER   (France)

^b HÔPITAL ROBERT DEBRÉ   (France)

^c HÔPITAL TENON   (France)

^d INSTITUT DE RECHERCHES INTERNATIONALES SERVIER   (France)

Author keywords

Agenesis of corpus callosum; Chromosomal rearrangement; Comparative genomic hybridization; De novo; Fluorescence in situ hybridization; Hypotonia; Trisomy 10p

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 10P; CHROMOSOME 6; CHROMOSOME ANALYSIS; CHROMOSOME PAINTING; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; CORPUS CALLOSUM AGENESIS; DNA HYBRIDIZATION; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; IMAGE ANALYSIS; KARYOTYPE; METAPHASE CHROMOSOME; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PARTIAL TRISOMY 10; PRIORITY JOURNAL; TELOMERE;

ADOLESCENT; CHROMOSOMES, HUMAN, PAIR 10; FEMALE; HUMANS; IN SITU HYBRIDIZATION; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; TRISOMY;

EID: 0031786138     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1998.5440412.x     Document Type: Article

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