Maria M Sasiadek - JoVE Visualize

Showing results (41-50 of 45) with videos related to

Pageof 5

Sort By:

You have reached the last page of results.This site can display upto 45 results.

Familial Cancer|October 21, 2017

Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and UkraineAleksander Myszka, Tu Nguyen-Dumont, Pawel Karpinski, et al.

BMC Medical Genetics|January 21, 2018

FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West UkraineTú Nguyen-Dumont, Aleksander Myszka, Pawel Karpinski, et al.

Human Molecular Genetics|August 21, 2018

Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexiaRobert Smigiel, Diane L Sherman, Malgorzata Rydzanicz, et al.

Genetics Research|August 11, 2020

Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?Tu Nguyen-Dumont, Pawel Karpinski, Maria M Sasiadek, et al.

European Journal of Human Genetics : EJHG|October 16, 2008

Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndromeThomas E Neumann, Judith Allanson, Ines Kavamura, et al.

Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 45 results.

Familial Cancer|October 21, 2017

Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and UkraineAleksander Myszka, Tu Nguyen-Dumont, Pawel Karpinski, et al.

BMC Medical Genetics|January 21, 2018

FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West UkraineTú Nguyen-Dumont, Aleksander Myszka, Pawel Karpinski, et al.

Human Molecular Genetics|August 21, 2018

Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexiaRobert Smigiel, Diane L Sherman, Malgorzata Rydzanicz, et al.

Genetics Research|August 11, 2020

Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?Tu Nguyen-Dumont, Pawel Karpinski, Maria M Sasiadek, et al.

European Journal of Human Genetics : EJHG|October 16, 2008

Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndromeThomas E Neumann, Judith Allanson, Ines Kavamura, et al.

Pageof 5