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Volumn 152 A, Issue 12, 2010, Pages 3154-3156
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Mosaic down syndrome in a patient with low-level mosaicism detected by microarray
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Author keywords
Down syndrome; Microarray; Mosaicism; SNP; Trisomy 21
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Indexed keywords
ARTICLE;
CASE REPORT;
CLINICAL FEATURE;
CLINODACTYLY;
DOWN SYNDROME;
DRY SKIN;
ECHOCARDIOGRAPHY;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
HUMAN;
KARYOTYPE;
MICROARRAY ANALYSIS;
MICROGNATHIA;
MOSAICISM;
NEWBORN;
NUCHAL TRANSLUCENCY MEASUREMENT;
PALPEBRAL FISSURE ANOMALY;
PATENT DUCTUS ARTERIOSUS;
PATENT FORAMEN OVALE;
PHALANX HYPOPLASIA;
PRENATAL SCREENING;
PRIORITY JOURNAL;
SINGLE NUCLEOTIDE POLYMORPHISM;
TRISOMY 21;
ANEUPLOIDY;
CHROMOSOMES, HUMAN, PAIR 21;
CYTOGENETIC ANALYSIS;
DNA;
DNA COPY NUMBER VARIATIONS;
DOWN SYNDROME;
FEMALE;
HUMANS;
INFANT, NEWBORN;
INTERPHASE;
MICROARRAY ANALYSIS;
MOSAICISM;
PHENOTYPE;
POLYMORPHISM, SINGLE NUCLEOTIDE;
TRISOMY;
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EID: 78649685698
PISSN: 15524825
EISSN: 15524833
Source Type: Journal
DOI: 10.1002/ajmg.a.33739 Document Type: Article |
Times cited : (16)
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References (5)
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