Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter

Congenital Anomalies

Volumn 49, Issue 2, 2009, Pages 85-88

  Yamada, Keitaro ^a,b,c   Uchiyama, Atsushi ^b   Arai, Mayuki ^b,c   Kubodera, Kuniko ^b,c   Yamamoto, Yutaka ^b,c   Orii, Koji O ^b,c   Nagasawa, Hiroyuki ^b   Masuno, Mitsuo ^d   Kohno, Yoshinori ^b  

^a RESEARCH INSTITUTE FOR MATERNAL AND CHILD HEALTH   (Japan)

^b GIFU PREFECTURAL GIFU HOSPITAL   (Japan)

^c GIFU UNIVERSITY   (Japan)

^d KAWASAKI UNIVERSITY OF MEDICAL WELFARE   (Japan)

Author keywords

16p13.3 distal monosomy; 16q22 distal trisomy; Chromosomal abnormality; Multiple anomalies; Upper airway stenosis

Indexed keywords

ANAMNESIS; ARTICLE; CASE REPORT; CHROMOSOME 16P; CHROMOSOME 16Q; CHROMOSOME ANALYSIS; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE SEVERITY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INFANT; LARYNX STENOSIS; MALE; PARTIAL MONOSOMY; PARTIAL TRISOMY; PRIORITY JOURNAL; UPPER AIRWAY STENOSIS; UPPER RESPIRATORY TRACT;

ADULT; AIRWAY OBSTRUCTION; CHROMOSOMES, HUMAN, PAIR 16; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; MONOSOMY; TRACHEAL STENOSIS; TRISOMY;

EID: 66949112210     PISSN: 09143505     EISSN: 17414520     Source Type: Journal    
DOI: 10.1111/j.1741-4520.2009.00228.x     Document Type: Article

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