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Clinical Genetics|October 12, 1999
FISH analysis with locus-specific probes in sperm from two translocation carrier menB Durak, Y H Ozön, M Ozdemir, et al.
American Journal of Human Genetics|January 1, 1994
Maternal uniparental disomy 22 has no impact on the phenotypeA A Schinzel, S Basaran, F Bernasconi, et al.
American Journal of Medical Genetics|May 1, 1989
Validity of cytogenetic analyses from trophoblast tissue throughout gestationP Miny, S Basaran, I H Pawlowitzki, et al.
Geburtshilfe Und Frauenheilkunde|May 1, 1986
[Prenatal diagnosis from chorionic villi: results in Münster]W Holzgreve, P Miny, S Basaran, et al.
Human Genetics|January 1, 1990
Molecular basis of beta-thalassemia in Turkey: detection of rare mutations by direct sequencingC Aulehla-Scholz, S Basaran, L Agaoglu, et al.
Balkan Journal of Medical Genetics : BJMG|April 5, 2021
Array-comparative Genomic Hybridization Results in Clinically Affected Cases with Apparently Balanced Chromosomal RearrangementsN B Satkin, B Karaman, S Ergin, et al.
American Journal of Medical Genetics|May 22, 1995
Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatallyP Miny, B Koppers, B Dworniczak, et al.
Pediatric Nephrology (Berlin, Germany)|October 25, 2000
Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish childrenI Bilge, H Kayserili, S Emre, et al.
American Journal of Human Genetics|February 1, 1994
A somatic origin of homologous Robertsonian translocations and isochromosomesW P Robinson, F Bernasconi, S Basaran, et al.
Genetics and Molecular Research : GMR|September 28, 2011
Association of serum sex steroid levels and bone mineral density with CYP17 and CYP19 gene polymorphisms in postmenopausal women in TurkeyM B Yilmaz, A Pazarbasi, A I Guzel, et al.
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