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Volumn 99, Issue 1, 2014, Pages 52-57
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Velopharyngeal insufficiency: High detection rate of genetic abnormalities if associated with additional features
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Author keywords
[No Author keywords available]
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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;
GENETICS;
SYNDROME;
VELOPHARYNGEAL INSUFFICIENCY;
CHILD;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 22;
COMPARATIVE GENOMIC HYBRIDIZATION;
DNA COPY NUMBER VARIATIONS;
FEMALE;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
MALE;
SPEECH DISORDERS;
VELOPHARYNGEAL INSUFFICIENCY;
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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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References (17)
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