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Human Genetics|November 1, 1994
Preliminary mutation analysis in the phenylalanine hydroxylase gene in Greek PKU and HPA patientsJ Traeger-Synodinos, E Kanavakis, M Kalogerakou, et al.
Genetic Counseling (Geneva, Switzerland)|August 5, 2009
Unilateral microtia in an infant with trisomy 18 mosaicismE Giannatou, H Leze, A Katana, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Long term follow up of a woman with classic form of Ehlers-Danlos syndrome associated with rare manifestations and review of the literatureS Kitsiou-Tzeli, E Leze, K Salavoura, et al.
Molecular and Cellular Probes|August 1, 1995
Identification of two novel mutations (296 + 1G-C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patientsM Tzetis, E Kanavakis, T Antoniadi, et al.
British Journal of Haematology|May 1, 1982
Globin gene mapping in normal Hb A2 types of beta-thalassaemiaE Kanavakis, A Metaxotou-Mavromati, C Kattamis, et al.
Molecular Syndromology|May 10, 2012
Severe Developmental Delay in a Patient with 7p21.1-p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene ClusterH Fryssira, P Makrythanasis, A Kattamis, et al.
Human Reproduction (Oxford, England)|January 5, 2002
Pregnancies following blastocyst stage transfer in PGD cycles at risk for beta-thalassaemic haemoglobinopathiesG A Palmer, J Traeger-Synodinos, S Davies, et al.
European Journal of Medical Genetics|September 15, 2011
Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3G Christopoulou, M Tzetis, A E Konstantinidou, et al.
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