A novel 22q11.2 microdeletion in DiGeorge syndrome.

American journal of human genetics

Volumn 64, Issue 2, 1999, Pages 659-667

  Rauch, A ^a   Pfeiffer, R A ^a   Leipold, G ^a   Singer, H ^a   Tigges, M ^a   Hofbeck, M ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CHILD; CHROMOSOME 22; CHROMOSOME DELETION; DIGEORGE SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; KARYOTYPING; LETTER; MALE; PEDIGREE; PHENOTYPE;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PEDIGREE; PHENOTYPE;

MLCS; MLOWN;

EID: 0033071959     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302235     Document Type: Letter

References (0)