Chromosome analysis of arsenic affected cattle

by S. Shekhar, A. K. Sahoo, N. Dalai, P. Chaudhary, P. K. Praveen, R. Saikhom, R. Rai
Published 2014-10-01

Karyotypes of <em>Nannospalax</em> (Palmer 1903) populations (Rodentia: Spalacidae) from centraleastern Anatolia, Turkey

by Yüksel Coskun, Servet Ulutürk, Alaettin Kaya
Published 2010-08-01

Cytogenetic Analysis for Suspected Chromosomal Abnormalities; A Five Years Experience

by Sunil Kumar Polipalli, Vijay Kumar Karra, Ankur Jindal, Madhavi Puppala, Pratiksha Singh, Kanchan Rawat, Seema Kapoor
Published 2016-09-01

Population Genetics of Latvians in the Context of Admixture between North-Eastern European Ethnic Groups

by Krūmiņa Astrīda, Pliss Liāna, Zariņa Gunita, Puzuka Agrita, Zariņa Agnese, Lāce Baiba, Elferts Didzis, Khrunin Andrey, Limborska Svetlana, Kloviņš Jānis, Gailīte Piekuse Linda
Published 2018-06-01

“Like sugar in milk”: reconstructing the genetic history of the Parsi population

by Gyaneshwer Chaubey, Qasim Ayub, Niraj Rai, Satya Prakash, Veena Mushrif-Tripathy, Massimo Mezzavilla, Ajai Kumar Pathak, Rakesh Tamang, Sadaf Firasat, Maere Reidla, Monika Karmin, Deepa Selvi Rani, Alla G. Reddy, Jüri Parik, Ene Metspalu, Siiri Rootsi, Kurush Dalal, Shagufta Khaliq, Syed Qasim Mehdi, Lalji Singh, Mait Metspalu, Toomas Kivisild, Chris Tyler-Smith, Richard Villems, Kumarasamy Thangaraj
Published 2017-06-01

Heterogeneous Patterns of Genetic Diversity and Differentiation in European and Siberian Chiffchaff (Phylloscopus collybita abietinus/P. tristis)

by Venkat Talla, Faheema Kalsoom, Daria Shipilina, Irina Marova, Niclas Backström
Published 2017-12-01

Variation of autosomes and X chromosome STR in breast cancer and gynecological cancer tissues

by Hou Youxiang, Dong Zhanfei, Kuerban Gulina
Published 2017-04-01

Culture shock

by Antoine Molaro, Harmit S Malik
Published 2017-12-01

The Non-random Location of Autosomal Genes That Participate in X Inactivation

by Barbara R. Migeon
Published 2019-08-01

Compound heterozygous dominant and recessive GJB2 mutations cause deafness with palmoplantar keratoderma

by Yasuhiro Arai, Masahiro Takahashi, Naoko Sakuma, Shin-Ya Nisio, Nobuhiko Oridate, Shin-Ichi Usami
Published 2017-01-01

SACS gene-related autosomal recessive spastic ataxia of Charlevoix-Saguenay from South India

by M Suraj Menon, C Velayudhan Shaji, K Abdulkhayar Kabeer, G Parvathy
Published 2016-01-01

Management of retinitis pigmentosa by Wharton’s jelly-derived mesenchymal stem cells: prospective analysis of 1-year results

by Emin Özmert, Umut Arslan
Published 2020-08-01

Clinical and genetic aspects of generalized aggressive periodontitis in families of Tumkur district of Karnataka, India

by Vaibhavi Joshipura, Shobha Krishna Subbaiah, Ravi Prakash Bdurga Saiprakash, Netravathi Thumbigere Dasakariyappa, B V Smitha, Mahantesha
Published 2013-01-01

Hereditary Ataxia

by Filiz Koc, Pinar Bengi Boz
Published 2009-06-01

Polycystic Kidney Disease

by Pedro Cena Rivero, Rocío Elizabeth Castillo Andrade, Silvia Marcela Baquero, Viviana Margarita Espirel
Published 2016-02-01

Infantile malignant osteopetrosis: A case report of three siblings

by Sahil Jain, Vineeta Pande, Geeta R Karambelkar, Sharad R Agarkhedkar
Published 2013-01-01

Mucopolysaccharidosis type I Hurler-Scheie syndrome: A rare case report

by Ramesh Tatapudi, M Gunashekhar, P Suryanarayana Raju
Published 2011-01-01

Progeria in siblings: A rare case report

by R Sowmiya, D Prabhavathy, S Jayakumar
Published 2011-01-01

CLINICO-RADIOLOGIC FEATURES OF BILATERAL MANDIBULAR SWELLING – A CASE REPORT OF CHERUBISM AND LITERATURE REVIEW

by Dysanoor Sujatha, Naik Shobha
Published 2012-09-01

Expression of Wilson's disease genomic locus

by Bochukova, Elena G.
Published 2003