• Reference :1

    Akyuz, B., Ertugrul, O., 2008. Detection of deficiency of uridine monophosphate synthase (DUMPS) in Holstein and native cattle in Turkey. Ankara Universitesi Veteriner Fakultesi Dergisi 55, 57–60.

    Akyuz, B., Bayram, D., Ertugrul, O., Iscan, K.M., 2008.  Turkiye’deyetiÅŸtirilenHolÅŸtaynvebazıyerlisıgırırkların da citrullinemiaallelininbelirlenmesi. Erciyes Universitesi Veteriner Fakultesi Dergisi 5, 17–20.

    Avanus, K.,  Altinel, A., 2017. Inherited diseases of Holstein cattle: Story so far in Turkey. Journal of Istanbul Veterinary Sciences. Volume 1, Issue 2, 40–46.

    Cole, J.B., Null, D.J., Vanraden, P.M., 2016. Phenotypic and genetic effects of recessive haplotypes on yield, longevity, and fertility. Journal of Dairy Science 99(9), 7274–7288.

    Citek, J., Blahova, B., 2004. Recessive disorders—a serious health hazard. Journal of Applied Biomedicine 2, 187–194.

    Citek, J., Rehout, V., Hajkova, J., Pavkova, J., 2006. Monitoring of the genetic health of cattle in the Czech Republic. Veterinary Medicine 51, 333–339

    Gholap, P.N., Kale, D.S., Sirothia, A.R., 2014. Genetic Diseases in Cattle: A ReviewRes. J. Animal, Veterinary and Fishery Science ISSN 2320 – 6535 2(2), 24–33.

    Grupe, S., Dietle, G., Schwerin, M., 1996. Population survey of citrullinaemia on German Holsteins. Livestock Production Science 45, 35–38.

    Gentry, P.A., Overton, K.M.,  Robinson, J.L., 1996. Bovine factor XI deficiency. Illinois Dairy Report,  32–35.

    Grupe, S., Dietl, G., Schwerin, M., 2006. Population survey of citrullinemia on German Holsteins. Livestock Production Science 45, 35–38.

    Jorgensen, C.B., Agerholm, J.S., Pedersen, J., Thomsen, P.D., 1993. Bovine leukocyte adhesion deficiency in Danish Holstein-Friesian cattle. PCR screening and allele frequency estimation. Acta Veterinaria Scandinavica 34, 231–236.

    Kociba, G.D., Ratnoff, O.D., Loeb, W.F., Wall, R.L., Heider, L.E., 1969. Bovine thromboplastin antecedent (factor XI) deficiency. Journal of Laboratory and Clinical Medicine 74, 37–41.

    Karslı, T., Sahin, E., Karslı, B.A., Alkan, S., Balcıoglu, M.S., 2011. Identification of alleles for factor XI (FXID) and uridine monophosphate synthase (DUMPS) deficiencies in Holstein cows reared in Antalya. Kafkas Universitesi Veteriner Fakultesi Dergisi 17, 503–505.

    Kaminski, S., Grzybowski, G., Prusak, B., Rusc, A., 2005. No incidence of DUMPS carriers in Polish dairy cattle. Journal of Applied Genetics 46, 395–397.

    Kristina, M., Renata, B., NijolÄ—, P., Rasa, U., 2019. Detection of bovine leukocyte adhesion deficiency, deficiency of uridine monophosphate synthase, and complex vertebral malformation in holstein cattle. Slovenian Veterinary Research 56(2), 75–82.

    Meydan, H., Yildiz, M.A., Agerholm, J.S., 2010. Screening for bovine leukocyte adhesion deficiency, deficiency of uridine monophosphate synthase, complex vertebral malformation, bovinecitrullinaemia and factor XI deficiency in Holstein cows reared in Turkey. Acta Veterinaria Scandinavica 52, 56 .

    Marron, B.M., Robinson, J.L., Gentry, P.A., Beever, J.E., 2004. Identification of a mutation associated with factor XI deficiency in Holstein cattle. Animal Genetics 35, 454–456.

    Meydan, H., 2017. Genetic Disorders and Control Strategies in Cattle Breeding (Editorial). Journal of Genetics and Mutation 1(1), 1.

    Norouzy, A., Nassiry, M.R., Eftekhari, S.F., Javadmanesh, A., Mohammad, A.M.R., Sulimova, G.E., 2005. Identification of bovine leukocyte adhesion deficiency (BLAD) carriers in Holstein and Brown Swiss AI bulls in Iran. Russian Journal of Genetics 41, 1409–1413.

    Oner, Y., Keskin, A., Elmaci, C., 2010. Identification of BLAD, DUMPS,citrullinaemia and factor XI deficiency in Holstein cattle in Turkey. Asian Journal of Animal and Veterinary Advances 5, 60–65.

    Patel, R.K., Kalpesh, J.S., Chauhan, J.B., Krishna, M.S., Singh, K.M., Sambasiva, R., 2007. Factor XI deficiency in Indian Bostaurus, Bosindicus, Bostaurusx Bosindicuscrossbreds and Bubalusbubalis. Genetics and Molecular Biology 30(3), 580–583.

    Ramesha, K.P., Alex, Rani, Rao, Akhila, Basavaraju, M, Haritha, P, Geetha, G.R., Kataktalware, M.A., Das, D.N., Jeyakumar, S., 2017a. Status of genetic disorders among indigenous and crossbred breeding bulls in India. Indian Journal of Biotechnology 16(1), 138–140.

    Ramesha, K. P., Rao, Akhila, Alex, Rani, Geetha, G.R., Basavaraju, M., Kataktalware, M.A., Das, D.N., Jeyakumar, S., 2017b. Screening for genetic disorders in indianmurrah and surti buffalo (Bubalus bubalis) bulls. Buffalo Bulletin 36(1), 133–142.

    Rajesh, K.P., Singh, K.M., Kalpesh, J.S., Chauhan, J.B., Krothapalli, R.S.,Rao, S., 2006. Lack of carriers of citrullinaemia and DUMPS in Indian Holstein cattle.Journal of Applied Genetics 47(3), 239–242.

    Robinson, J.L., Burns, J.L., Magura, C.E., Shanks, R.D., 1993. Low incidence of citrullinaemia carriers among dairy cattle of the United States. Journal of Dairy Science 76, 853–858.

    Sambrook, J., Russell, D.W., 1989. Preparation and analysis of eukaryotic DNA. In: Molecular Cloning: A Laboratory Manual. 3rd Edition. Cold Spring Harbor Laboratory Press, New York: 6.1-6.62]

    KorkmazAgaoglu, O., Agaoglu, A.R., Saatci, M., 2015. Estimating allele frequencies of some hereditary diseases in Holstein cattle reared in Burdur Province, Turkey. Turkish Journal of Veterinary and Animal Sciences 39, 338–342.

    Virgen-Mendez, A., Ayala-Valdovinos, M.A., Galindo-Garcia, J., Sanchez-Chipres, D.R., Lemus-Flores, C.,  Duifhuis-Rivera, T., 2019. Carrier frequency of autosomal recessive disorders (BC, BLAD, FXID and CVM) in Holstein cows in Jalisco, Mexico. RevistaPesquisaVeterináriaBrasileira (Brazilian Journal of Veterinary Research) 39(7), 481–484. 

    Mondal, K., Chakravarti, S., Ghosh, A.K., Kumar, S., Nayak, B., Nandiu, S., Sarkar, U., Deb, R., De, A., Biswas, J., 2016. Novel identification of Factor XI deficiency in Indian Sahiwal (Bosindicus) cattle. Molecular Biology Reports 43(4), 213–219. doi: 10.1007/s11033-016-3955-5..

    Gebreselassie, G., De, S.,  Mukherje, A., Gohain, M., 2019. Genotyping of Indian cattle for common genetic disorders: Deficiency of Uridine Monophosphate Synthase and Factor XI. Academia Journal of Biotechnology 7(5), 084–090.

People also read

Research Article

The Role of Parkland for Conservation of Useful Plant Species Diversity in Arba Minch, Southern Ethiopia

Mulugeta Kebebew

Parkland, paradise lodge, diversity, useful plant, Ethiopia

Published Online : 13 May 2019

Review Article

Occurrence of Acaricidal Resistance on Ticks and Their Detection Measures

J. K. Chamuah, Amenti and Lalchamliani

Ectoparasite, tick, acaricide resistance, treatment 

Published Online : 01 Jun 2020