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Pediatrics CRA
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Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.
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Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.
Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation. Am J Med Genet A. 2006 Mar 01; 140(5):442-52.
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PubMed
subject areas
Alleles
Autoantigens
Child, Preschool
Chromosome Banding
Chromosomes, Human, Pair 15
Chromosomes, Human, X
DNA Methylation
Female
Genotype
Humans
In Situ Hybridization, Fluorescence
Karyotyping
Long Interspersed Nucleotide Elements
Male
Microsatellite Repeats
Pedigree
Phenotype
Ribonucleoproteins, Small Nuclear
snRNP Core Proteins
Translocation, Genetic
Trisomy
authors with profiles
PAWEL STANKIEWICZ
JAMES LUPSKI