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Antoni Pyrkosz

Showing results (11-20 of 16) with videos related to

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Ginekologia Polska|September 10, 2005
[Fetal warfarin syndrome in twin pregnancy]Barbara Królak-Olejnik, Antoni Pyrkosz, Jerzy Lagan, et al.
Pediatric Radiology|March 4, 2003
Schimke immuno-osseous dysplasia: two casesAnna Tylki-Szymańska, Antoni Pyrkosz, Małgorzata Krajewska-Walasek, et al.
Gene|May 25, 2013
Apolipoprotein E genotype and LRP1 polymorphisms in patients with different clinical types of metachromatic leukodystrophyAgnieszka Ługowska, Małgorzata Musielak, Ewa Jamroz, et al.
Journal of Human Genetics|January 15, 2016
Variable expressivity of the phenotype in two families with brachydactyly type E, craniofacial dysmorphism, short stature and delayed bone age caused by novel heterozygous mutations in the PTHLH geneAleksander Jamsheer, Anna Sowińska-Seidler, Ewelina M Olech, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Comprehensive genomic analysis of patients with disorders of cerebral cortical developmentWojciech Wiszniewski, Pawel Gawlinski, Tomasz Gambin, et al.
Genes|December 24, 2021
Exome Sequencing Reveals Novel Variants and Expands the Genetic Landscape for Congenital MicrocephalyMateusz Dawidziuk, Tomasz Gambin, Ewelina Bukowska-Olech, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Ginekologia Polska|September 10, 2005
[Fetal warfarin syndrome in twin pregnancy]Barbara Królak-Olejnik, Antoni Pyrkosz, Jerzy Lagan, et al.
Pediatric Radiology|March 4, 2003
Schimke immuno-osseous dysplasia: two casesAnna Tylki-Szymańska, Antoni Pyrkosz, Małgorzata Krajewska-Walasek, et al.
Gene|May 25, 2013
Apolipoprotein E genotype and LRP1 polymorphisms in patients with different clinical types of metachromatic leukodystrophyAgnieszka Ługowska, Małgorzata Musielak, Ewa Jamroz, et al.
Journal of Human Genetics|January 15, 2016
Variable expressivity of the phenotype in two families with brachydactyly type E, craniofacial dysmorphism, short stature and delayed bone age caused by novel heterozygous mutations in the PTHLH geneAleksander Jamsheer, Anna Sowińska-Seidler, Ewelina M Olech, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Comprehensive genomic analysis of patients with disorders of cerebral cortical developmentWojciech Wiszniewski, Pawel Gawlinski, Tomasz Gambin, et al.
Genes|December 24, 2021
Exome Sequencing Reveals Novel Variants and Expands the Genetic Landscape for Congenital MicrocephalyMateusz Dawidziuk, Tomasz Gambin, Ewelina Bukowska-Olech, et al.
Pageof 2