Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome;Heterogeneidad de la presentación clínica del síndrome de microdeleción del cromosoma 22, región q11

Revista Medica de Chile

Volumn 129, Issue 5, 2001, Pages 515-521

  Muñoz C , Sebastián ^a   Garay G , Francisco ^a   Flores C , Ingrid ^a   Heusser R , Felipe ^a   Talesnik G , Eduardo ^a   Aracena A , Mariana ^a   Mellado S , Cecilia ^a   Méndez R , Cecilia ^a   Arnaiz G , Pilar ^a   Repetto L , Gabriela ^a  

^a HOSPITAL DR SÓTERO DEL RÍO   (Chile)

Author keywords

Abnormalities; Chromosome abnormalities; Chromosome deletion; DiGeorge syndrome

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 14; CHROMOSOME 22; CHROMOSOME DELETION; DIGEORGE SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; KARYOTYPING; MALE; NEWBORN; PRESCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE;

EID: 0035350258     PISSN: 00349887     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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