No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585 [2]

American Journal of Medical Genetics

Volumn 83, Issue 5, 1999, Pages 425-426

  Bartsch, O ^a   Wagner, A ^a   Hinkel, G K ^a   Lichtner, P ^a   Murken, J ^a   Schuffenhauer, S ^a  

^a UNIVERSITY HOSPITAL CARL GUSTAV CARUS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHILD; CHROMOSOME 10P; CONGENITAL HEART DISEASE; DIGEORGE SYNDROME; FACE MALFORMATION; GENE DELETION; GENE LOCUS; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; LETTER; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL;

CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 10; DIGEORGE SYNDROME; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE;

EID: 0033597384     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990423)83:5<425::AID-AJMG17>3.0.CO;2-Q     Document Type: Letter

References (7)