Videonasopharyngoscopy in patients with 22q11.2 deletion syndrome (Shprintzen syndrome)

International Journal of Pediatric Otorhinolaryngology

Volumn 67, Issue 8, 2003, Pages 911-915

  Ysunza, Antonio ^a   Pamplona, M C ^a   Ramírez, Elena ^a   Canún, Sonia ^a   Sierra, M C ^a   Silva Rojas, Andres ^b  

^a HOSPITAL GENERAL DR MANUEL GEA GONZÁLEZ   (Mexico)

^b HOSPITAL GENERAL DE MÉXICO   (Mexico)

Author keywords

22q11.2 Deletion; Cleft palate; Internal carotid artery; Shprintzen syndrome; Submucous cleft palate; Velo cardio facial syndrome; Videonasopharyngoscopy

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLEFT PALATE; CLINICAL ARTICLE; CONTROLLED STUDY; DIAGNOSTIC APPROACH ROUTE; DIAGNOSTIC IMAGING; DIAGNOSTIC VALUE; DOUBLE BLIND PROCEDURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INTERMETHOD COMPARISON; MALE; MEDICAL ASSESSMENT; PRIORITY JOURNAL; PULSATILE FLOW; SUBMUCOSA; VELOCARDIOFACIAL SYNDROME; VIDEONASOPHARYNGOSCOPY;

EID: 0043171041     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-5876(03)00157-5     Document Type: Article

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