DiGeorge syndrome with discordant phenotype in monozygotic twins.

Journal of medical genetics

Volumn 37, Issue 9, 2000, Pages

  Hillebrand, G ^a   Siebert, R ^a   Simeoni, E ^a   Santer, R ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 22; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; DIGEORGE SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; INFANT; KARYOTYPING; MALE; MONOZYGOTIC TWINS; NOTE; PATHOLOGY; PHENOTYPE;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; PHENOTYPE; TWINS, MONOZYGOTIC;

MLCS; MLOWN;

EID: 0034267728     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.37.9.e23     Document Type: Note

References (0)