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
Sko Steve Madden, Inuikii, Ilse Jacobsen, Gaimo, Marco Tozzi Beige - Dame- Risør Sko - Risør
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Advanced genome-wide screening in human genomic disorders
The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chrom
2009 Vienna - European Society of Human Genetics
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
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
17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction
17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction | Journal of Medical Genetics
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Bisgaard Chelseastøvle Elvira Sort – Twenty20.dk
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Microarray Comparative Genome Hybridization in mental retardation / congenital malformations
17q21.31 microduplication patients are characterized by behavioural problems and poor social interaction.
Damesko – Page 3 – Twenty20.dk
Billi Bi loafer m.frynser sort
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Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a s
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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
PDF) Further delineation of the 15q13 microdeletion and duplication syndromes: A clinical spectrum varying from non-pathogenic to a severe outcome
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The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chrom
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