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S Aftimos

Showing results (21-30 of 26) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|January 29, 2010
13q33.2 deletion: a rare cause of ambiguous genitalia in a male newborn with growth restrictionJ H Andresen, S Aftimos, E Doherty, et al.
Genetics and Molecular Research : GMR|September 17, 2010
Molecular characterisation of a der(Y)t(Xp;Yp) with Xp functional disomy and sex reversalF Ashton, R O'Connor, J M Love, et al.
Journal of Medical Genetics|February 24, 2001
Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasiaS P Robertson, D J Shears, P Oei, et al.
British Journal of Biomedical Science|June 29, 2011
Chromosome microarray analysis in a clinical environment: new perspective and new challengeA George, R Marquis-Nicholson, L T Zhang, et al.
Journal of Medical Genetics|May 19, 2009
Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndromeT Y Tan, S Aftimos, L Worgan, et al.
Nature Genetics|November 5, 1997
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domainR J Gibbons, S Bachoo, D J Picketts, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Acta Paediatrica (Oslo, Norway : 1992)|January 29, 2010
13q33.2 deletion: a rare cause of ambiguous genitalia in a male newborn with growth restrictionJ H Andresen, S Aftimos, E Doherty, et al.
Genetics and Molecular Research : GMR|September 17, 2010
Molecular characterisation of a der(Y)t(Xp;Yp) with Xp functional disomy and sex reversalF Ashton, R O'Connor, J M Love, et al.
Journal of Medical Genetics|February 24, 2001
Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasiaS P Robertson, D J Shears, P Oei, et al.
British Journal of Biomedical Science|June 29, 2011
Chromosome microarray analysis in a clinical environment: new perspective and new challengeA George, R Marquis-Nicholson, L T Zhang, et al.
Journal of Medical Genetics|May 19, 2009
Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndromeT Y Tan, S Aftimos, L Worgan, et al.
Nature Genetics|November 5, 1997
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domainR J Gibbons, S Bachoo, D J Picketts, et al.
Pageof 3