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BMC Medical Genetics|November 17, 2016
Clinical utility of array comparative genomic hybridisation in prenatal settingLuca Lovrecic, Ziga Iztok Remec, Marija Volk, et al.
Croatian Medical Journal|September 15, 2005
Molecular analysis in diagnostic procedure of hearing impairment in newbornsSanja Zaputovic, Tea Stimac, Igor Prpic, et al.
Plos One|June 9, 2021
Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centreIvana Babić Božović, Aleš Maver, Lea Leonardis, et al.
Biomedical Reports|January 6, 2022
Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta-analysisNada Starčević Čizmarević, Božena Ćurko-Cofek, Vesna Barac-Latas, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|July 2, 2005
Hemochromatosis-causing mutations C282Y and H63D are not risk factors for atherothrombotic cerebral infarctionHelena Hruskovicová, Tomaz Milanez, Jan Kobal, et al.
Croatian Medical Journal|June 13, 2024
Pregnant couples' attitude toward extended pre-conceptional genomic screeningMojca Čižek Sajko, Bernarda Prosenc, Lovro Vidmar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 11, 2021
Children with cavernous malformations of the central nervous systemUla Arkar, Tina Vipotnik Vesnaver, Aleš Maver, et al.
Plos One|March 26, 2013
Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertilityAlenka Hodžić, Momčilo Ristanović, Branko Zorn, et al.
International Journal of Molecular Sciences|March 6, 2021
Stationary and Progressive Phenotypes Caused by the p.G90D Mutation in Rhodopsin GeneNina Kobal, Tjaša Krašovec, Maja Šuštar, et al.
Medicinski Arhiv|January 10, 2003
[The DNA test in the diagnosis of Huntington disease]Rifet Terzić, Emir Tupković, Natasa Logar, et al.
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