Chromosome 5q-syndrome - ENT pathologies;Chromosom-5q-syndrom aus HNO-ärztlicher sicht

Laryngo- Rhino- Otologie

Volumn 81, Issue 8, 2002, Pages 565-567

  Harréus, Ulrich A ^a   Issing, W J ^a  

^a UNIVERSITY OF MUNICH   (Germany)

Author keywords

Chromosome 5; Deformity; Hearing loss; Otolaryngology

Indexed keywords

ARTICLE; BLOOD DISEASE; CASE REPORT; CHROMOSOME 5Q; CHROMOSOME DELETION; FEMALE; HEARING LOSS; HUMAN; INFANT; LARYNGOMALACIA; PRIORITY JOURNAL; SKELETON MALFORMATION; SYNDROME;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 5; COCHLEA; DEAFNESS; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; FEMALE; HUMANS; INFANT; LARYNGEAL DISEASES; OTOACOUSTIC EMISSIONS, SPONTANEOUS; SYNDROME; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0036676304     PISSN: 09358943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-33361     Document Type: Article

References (7)

1. Distinct hëmatological disorder with deletion of long arm of No. 5 chromosome
2. The 5q-abnormality
3. The 5q-syndrome: A scientific and clinical update
4. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins (8;5) (p23;q33q35)
5. Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly
6. Clinical manifestations of trisomy 5q
7. A case of de novo interstitial deletion of chromosome 5 (q33q34)