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Microarray Comparative Genome Hybridization in mental retardation / congenital malformations
PDF) 17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction
Intellectual disability secondary to a 16p13 duplication in a 1;16 translocation. Extended phenotype in a four‐generation family - Mohamed - 2015 - American Journal of Medical Genetics Part A - Wiley Online Library
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Thesis Cover.cdr
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17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction
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PDF) Further delineation of the 15q13 microdeletion and duplication syndromes: A clinical spectrum varying from non-pathogenic to a severe outcome
GENETIC STUDIES IN DEVELOPMENTAL SKELETAL AND LIMB DEFECTS
17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction | Journal of Medical Genetics
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Advanced genome-wide screening in human genomic disorders
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a s
Improving our insight in the genetic origin of congenital heart defects using array comparative genome hybridization
Bisgaard Chelseastøvle Elvira Sort – Twenty20.dk
Intellectual disability secondary to a 16p13 duplication in a 1;16 translocation. Extended phenotype in a four‐generation family - Mohamed - 2015 - American Journal of Medical Genetics Part A - Wiley Online Library
Intellectual disability secondary to a 16p13 duplication in a 1;16 translocation. Extended phenotype in a four‐generation family - Mohamed - 2015 - American Journal of Medical Genetics Part A - Wiley Online Library
Intellectual disability secondary to a 16p13 duplication in a 1;16 translocation. Extended phenotype in a four‐generation family - Mohamed - 2015 - American Journal of Medical Genetics Part A - Wiley Online Library
The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chrom
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