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Volumn 167, Issue 11, 2015, Pages 2839-2843

Intellectual disability and overgrowth-A new case of 19p13.13 microdeletion syndrome with digital abnormalities

Author keywords

19p13.13 microdeletion; Finger pads; Intellectual disability; NFIX; Overgrowth

Indexed keywords

AMNIOCENTESIS; ARTICLE; ATAXIC GAIT; BODY HEIGHT; BODY WEIGHT; BONE AGE; BRAIN DISEASE; CACNA1A GENE; CALR GENE; CASE REPORT; CAUCASIAN; CHILD; CHROMOSOME 19P; CHROMOSOME DELETION; DAND5 GENE; DEHYDRATION; DNASE2 GENE; FACE DYSMORPHIA; FARSA GENE; FEMALE; FINGER MALFORMATION; FUNNEL CHEST; GADD45GIP1 GENE; GAIT DISORDER; GCDH GENE; GENE; GENETIC IDENTIFICATION; GROWTH DISORDER; HEAD CIRCUMFERENCE; HUMAN; HYPERNATREMIA; IER2 GENE; INTELLECTUAL IMPAIRMENT; JUNB GENE; KARYOTYPE; KIAA0973 GENE; KLF1 GENE; LANGUAGE DELAY; LYL1 GENE; MACROGLOSSIA; MAST1 GENE; METABOLIC ACIDOSIS; MICRODELETION SYNDROME; MUSCLE HYPOTONIA; NACC1 GENE; NEWBORN INTENSIVE CARE; NFIX GENE; NUCLEAR MAGNETIC RESONANCE IMAGING; NYSTAGMUS; OPHTHALMOLOGY; PRDX2 GENE; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; RAD23A GENE; RNASEH2A GENE; RTBDN GENE; SP1 GENE; STRABISMUS; STX10 GENE; SYCE2 GENE; TRMT1 GENE; VENTRICULOMEGALY; CHROMOSOME 19; CHROMOSOME ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; COMPLICATION; CONGENITAL MALFORMATION; FINGER; GENETICS; GROWTH, DEVELOPMENT AND AGING; INFANT; NEWBORN; PRESCHOOL CHILD; SYNDROME;

EID: 84944811001     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.37280     Document Type: Article
Times cited : (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.