Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2

Journal of Medical Genetics

Volumn 37, Issue 6, 2000, Pages 452-454

  Trost, D ^a   Wiebe, W ^a   Uhlhaas, S ^a   Schwindt, P ^a   Schwanitz, G ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 22Q; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CONTROLLED STUDY; DIGEORGE SYNDROME; DNA FLANKING REGION; FAMILY STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HAPLOTYPE; HUMAN; LETTER; MARKER GENE; MEIOSIS; PEDIGREE ANALYSIS; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SOMATIC CROSSING OVER; VELOCARDIOFACIAL SYNDROME;

EID: 0034081868     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.37.6.452     Document Type: Letter

References (19)