Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Acta Clinica Belgica|June 24, 2015
Prevalence and risk factors of low bone mineral density in patients with multiple sclerosisI Coskun Benlidayi, S Basaran, A Evlice, et al.
Prenatal Diagnosis|July 1, 1986
Inv dup (15): prenatal diagnosis and postnatal follow-upP Miny, S Basaran, E Kuwertz, et al.
American Journal of Medical Genetics. Part A|December 6, 2011
Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutationsHülya Kayserili, U Altunoglu, H Ozgur, et al.
Prenatal Diagnosis|May 1, 1988
Rapid karyotyping for prenatal diagnosis in the second and third trimesters of pregnancyS Basaran, P Miny, I H Pawlowitzki, et al.
Molecular Syndromology|April 10, 2014
Novel indel Mutation in the GDF5 Gene Is Associated with Brachydactyly Type C in a Four-Generation Turkish FamilyZ O Uyguner, M Kocaoğlu, G Toksoy, et al.
Cytogenetic and Genome Research|October 23, 2003
Parental origin of the two additional haploid sets of chromosomes in an embryo with tetraploidyA Baumer, D Dres, S Basaran, et al.
American Journal of Human Genetics|February 1, 1992
No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangementsA A Schinzel, P A Adelsberger, F Binkert, et al.
Geburtshilfe Und Frauenheilkunde|May 1, 1986
[Chromosome studies of chorionic villi: experiences following 118 diagnostic interventions]P Miny, W Holzgreve, S Basaran, et al.
Nigerian Journal of Clinical Practice|December 12, 2013
Effect of the number of portal area on modified histological activity index of viral hepatitis and histological findingsM Gurbuzel, G Saygi, F Ozyigit, et al.
Cytogenetic and Genome Research|September 29, 2007
Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy maleA Baumer, S Basaran, M Taralczak, et al.
Pageof 3