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Volumn 99, Issue 1, 2014, Pages 52-57

Velopharyngeal insufficiency: High detection rate of genetic abnormalities if associated with additional features

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; AORTA COARCTATION; ASPERGER SYNDROME; ATTENTION DEFICIT DISORDER; BIFID UVULA; CHILD; CHILDHOOD DISEASE; CHROMOSOME DELETION 22Q11; CLINICAL ARTICLE; CLINICAL GENETICS; CLINODACTYLY; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; COPY NUMBER VARIATION; CRYPTORCHISM; FACE DYSMORPHIA; FAMILY COUNSELING; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GASTROESOPHAGEAL REFLUX; GENETIC DISORDER; GENETIC SCREENING; GENETIC TRAIT; HEARING IMPAIRMENT; HEART ATRIUM SEPTUM DEFECT; HEART MURMUR; HIGH MYOPIA; HUMAN; HYDROCELE; HYPERMETROPIA; HYPERNASALITY; HYPOCALCEMIA; HYPOTHYROIDISM; IMPULSIVENESS; JOINT LAXITY; LANGUAGE DELAY; LEARNING DISORDER; LUNG MALFORMATION; MALE; MICROARRAY ANALYSIS; MICROCEPHALY; MUSCLE HYPOTONIA; NASAL SPEECH; OBSESSIVE COMPULSIVE DISORDER; PALATE MALFORMATION; PALATOPHARYNGEAL INCOMPETENCE; PATENT DUCTUS ARTERIOSUS; PATIENT REFERRAL; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PULMONARY VALVE STENOSIS; REVIEW; SCHOOL CHILD; SEIZURE; SHORT STATURE; SPEECH DELAY; SPEECH DISORDER; STRABISMUS;

EID: 84890571933     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/archdischild-2013-304484     Document Type: Review
Times cited : (5)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.