Microdeletion 22q11.2: Clinical data and deletion size [4]

Journal of Medical Genetics

Volumn 36, Issue 9, 1999, Pages 721-723

  Kerstjens Frederikse, W S ^a   Kurahashi, H ^a   Driscoll, D A ^a   Budarf, M L ^a   Emanuel, B S ^a   Beatty, B ^a   Scheidl, T ^a   Siegel Bartelt, J ^a   Henderson, K ^a   Cytrynbaum, C ^a   Nie, G ^a   Teshima, I ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INFANT; KARYOTYPING; LETTER; MAJOR CLINICAL STUDY; MALE; MULTIPLE MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; MALE; NOSE; PALATE;

EID: 0032876129     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (14)