Search research articles
Contact Us
Filters
Showing results (131-140 of 274) with videos related to
Page
of 28
Sort By:
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics
|
December 2, 2024
Maternal genetic risk factors for spontaneous preterm birth: A systematic review and meta-analysis
Tea Mladenić, Anita Barišić, Nina Pereza, et al.
European Journal of Human Genetics : EJHG
|
February 18, 2025
Towards a patient-centred classification of genetic disease severity
Mojca Cizek Sajko, Lovro Vidmar, Bernarda Prosenc, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)
|
October 10, 2007
Polymorphisms in the interleukin-12/18 genes and recurrent spontaneous abortion
Sasa Ostojić, Marija Volk, Igor Medica, et al.
Clinical Genetics
|
June 11, 2024
Non-dilated left ventricular cardiomyopathy with arrhythmias is commonly caused by the nonsense variant DSP:c.3793G>T in Slovenian patients
Nina Vodnjov, Anja Zupan Mežnar, Aleš Maver, et al.
BMC Medical Genetics
|
November 17, 2016
Clinical utility of array comparative genomic hybridisation in prenatal setting
Luca Lovrecic, Ziga Iztok Remec, Marija Volk, et al.
Croatian Medical Journal
|
September 15, 2005
Molecular analysis in diagnostic procedure of hearing impairment in newborns
Sanja Zaputovic, Tea Stimac, Igor Prpic, et al.
Plos One
|
June 9, 2021
Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centre
Ivana 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-analysis
Nada 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 infarction
Helena Hruskovicová, Tomaz Milanez, Jan Kobal, et al.
Croatian Medical Journal
|
June 13, 2024
Pregnant couples' attitude toward extended pre-conceptional genomic screening
Mojca Čižek Sajko, Bernarda Prosenc, Lovro Vidmar, et al.
Page
of 28
Search research articles
Search
Showing results (131-140 of 274) with videos related to
Sort By:
Page
of 28
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics
|
December 2, 2024
Maternal genetic risk factors for spontaneous preterm birth: A systematic review and meta-analysis
Tea Mladenić, Anita Barišić, Nina Pereza, et al.
European Journal of Human Genetics : EJHG
|
February 18, 2025
Towards a patient-centred classification of genetic disease severity
Mojca Cizek Sajko, Lovro Vidmar, Bernarda Prosenc, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)
|
October 10, 2007
Polymorphisms in the interleukin-12/18 genes and recurrent spontaneous abortion
Sasa Ostojić, Marija Volk, Igor Medica, et al.
Clinical Genetics
|
June 11, 2024
Non-dilated left ventricular cardiomyopathy with arrhythmias is commonly caused by the nonsense variant DSP:c.3793G>T in Slovenian patients
Nina Vodnjov, Anja Zupan Mežnar, Aleš Maver, et al.
BMC Medical Genetics
|
November 17, 2016
Clinical utility of array comparative genomic hybridisation in prenatal setting
Luca Lovrecic, Ziga Iztok Remec, Marija Volk, et al.
Croatian Medical Journal
|
September 15, 2005
Molecular analysis in diagnostic procedure of hearing impairment in newborns
Sanja Zaputovic, Tea Stimac, Igor Prpic, et al.
Plos One
|
June 9, 2021
Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centre
Ivana 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-analysis
Nada 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 infarction
Helena Hruskovicová, Tomaz Milanez, Jan Kobal, et al.
Croatian Medical Journal
|
June 13, 2024
Pregnant couples' attitude toward extended pre-conceptional genomic screening
Mojca Čižek Sajko, Bernarda Prosenc, Lovro Vidmar, et al.
Page
of 28