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Magdalena Chmara

Showing results (21-30 of 25) with videos related to

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Genes, Chromosomes & Cancer|July 11, 2006
Somatic loss of wild type NF1 allele in neurofibromas: Comparison of NF1 microdeletion and non-microdeletion patientsThomas De Raedt, Ophélia Maertens, Magdalena Chmara, et al.
Life (Basel, Switzerland)|November 7, 2020
Monitoring the Effects of Hypolipidemic Treatment in Children with Familial Hypercholesterolemia in PolandMatylda Hennig, Agnieszka Brandt-Varma, Anna Wołoszyn-Durkiewicz, et al.
Nature Genetics|August 21, 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotypeHilde Brems, Magdalena Chmara, Mourad Sahbatou, et al.
Cardiology Journal|February 11, 2022
Effectiveness and safety of PCSK9 inhibitor therapy in patients with familial hypercholesterolemia within a therapeutic program in Poland: Preliminary multicenter dataKrzysztof Chlebus, Barbara Cybulska, Piotr Dobrowolski, et al.
Human Mutation|November 20, 2010
Legius syndrome in fourteen familiesEllen Denayer, Magdalena Chmara, Hilde Brems, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Genes, Chromosomes & Cancer|July 11, 2006
Somatic loss of wild type NF1 allele in neurofibromas: Comparison of NF1 microdeletion and non-microdeletion patientsThomas De Raedt, Ophélia Maertens, Magdalena Chmara, et al.
Life (Basel, Switzerland)|November 7, 2020
Monitoring the Effects of Hypolipidemic Treatment in Children with Familial Hypercholesterolemia in PolandMatylda Hennig, Agnieszka Brandt-Varma, Anna Wołoszyn-Durkiewicz, et al.
Nature Genetics|August 21, 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotypeHilde Brems, Magdalena Chmara, Mourad Sahbatou, et al.
Cardiology Journal|February 11, 2022
Effectiveness and safety of PCSK9 inhibitor therapy in patients with familial hypercholesterolemia within a therapeutic program in Poland: Preliminary multicenter dataKrzysztof Chlebus, Barbara Cybulska, Piotr Dobrowolski, et al.
Human Mutation|November 20, 2010
Legius syndrome in fourteen familiesEllen Denayer, Magdalena Chmara, Hilde Brems, et al.
Pageof 3