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Journal of Applied Genetics|May 10, 2006
Adjustments for heterogeneous herd-year variances in a random regression model for genetic evaluations of Polish Black-and-White cattleTomasz Strabel, Tomasz Jankowski, Janusz JamrozikJournal of Applied Genetics|May 10, 2006
A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?Adrianna Mostowska, Barbara Biedziak, Wiesław H TrzeciakJournal of Applied Genetics|May 10, 2006
Trends in diagnosis and prevalence of critical congenital heart defects in the Podkarpacie province in 2002-2004, based on data from the Polish Registry of Congenital MalformationsAneta Górska-Kot, Witold Błaz, Ewa Pszeniczna, et al.Journal of Applied Genetics|August 1, 2006
Chromosome pairing in triploid intergeneric hybrids of Festuca pratensis with Lolium multiflorum, revealed by GISHArkadiusz Kosmala, Elzbieta Zwierzykowska, Zbigniew ZwierzykowskiJournal of Applied Genetics|August 1, 2006
Lack of carriers of citrullinaemia and DUMPS in Indian Holstein cattleRajesh K Patel, Krishna M Singh, Kalpesh J Soni, et al.Journal of Applied Genetics|February 3, 2007
Exploration of genetic diversity among Xinjiang Triticum and Triticum polonicum by AFLP markersMasum A S M G Akond, Nobuyoshi Watanabe, Yoshihiko FurutaJournal of Applied Genetics|February 3, 2007
EST-SSR DNA polymorphism in durum wheat (Triticum durum L.) collectionsHan-Yan Wang, Yu-Ming Wei, Ze-Hong Yan, et al.Journal of Applied Genetics|February 3, 2007
Methods of minimal residual disease (MRD) detection in childhood haematological malignanciesJustyna Jółkowska, Katarzyna Derwich, Małgorzata DawidowskaJournal of Applied Genetics|February 3, 2007
De novo complex chromosomal rearrangement of 46, XY, t (3; 16; 8) (p26; q13; q21.2) in a non-obstructive azoospermic maleIman Salahshourifar, Mohammad Ali Sedighi Gilani, Ahmad Vosough, et al.Journal of Applied Genetics|December 31, 2022
A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism-a case report and literature review of the partial 16p13.3 trisomy syndromeMagdalena Socha, Anna Szoszkiewicz, Dorota Simon, et al.Pageof 163