Anterior laryngeal webs and 22q11 deletions [1]

American Journal of Medical Genetics

Volumn 79, Issue 2, 1998, Pages 152-

  Stoler, J M ^a   Ladoulis, M ^a   Holmes, L B ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; DISEASE ASSOCIATION; GLOTTIS; HUMAN; LARYNX DISORDER; LETTER; MALE; MALFORMATION SYNDROME; NEWBORN; PRESCHOOL CHILD; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 22; GENE DELETION; HUMANS; INFANT, NEWBORN; LARYNGEAL DISEASES; LARYNX; MALE;

EID: 0032169056     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980901)79:2<152::AID-AJMG12>3.0.CO;2-I     Document Type: Letter

References (8)