Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Beata Skoczylas"'
Autor:
Hanna Moczulska, Michal Pietrusinski, Karolina Zezawska, Marcin Serafin, Beata Skoczylas, Tomasz Jachymski, Katarzyna Wojda, Piotr Sieroszewski, Maciej Borowiec
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Objective: Tetrasomy 9p and trisomy 9p are rare chromosomal aberrations. The phenotypes of tetrasomy 9p and trisomy 9p are variable. Most cases are diagnosed in the postnatal period. The study aims to analyze the prenatal phenotype of tetrasomy 9p an
Externí odkaz:
https://doaj.org/article/eeb2474cf19d49c6b065f0309e221e99
Autor:
Hanna Moczulska, Marta Chrzanowska-Steglinska, Beata Skoczylas, Katarzyna Wojda, Maciej Borowiec, Piotr Sieroszewski
Publikováno v:
Ginekologia Polska.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3aa912c13cefe6b7c79a061c55772f6
https://doi.org/10.5603/gp.a2022.0143
https://doi.org/10.5603/gp.a2022.0143
Autor:
Hanna Moczulska, Michal Pietrusinski, Marcin Serafin, Beata Skoczylas, Piotr Sieroszewski, Maciej Borowiec
Publikováno v:
The application of clinical genetics. 15
Hanna Moczulska,1 Michal Pietrusinski,1 Marcin Serafin,1 Beata Skoczylas,1 Piotr Sieroszewski,2 Maciej Borowiec1 1Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland; 2Department of Fetal Medicine and Gynecology, Medical Univers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4144552fd940fd3bc4e0f3e97ae12d4b
https://pubmed.ncbi.nlm.nih.gov/36213554
https://pubmed.ncbi.nlm.nih.gov/36213554
Autor:
Karolina Antosik, Marta Chrzanowska Steglińska, Michał Pietrusiński, Hanna Moczulska, Marta Kacprzak, Piotr Sieroszewski, Paulina Jakiel, Beata Skoczylas, Maciej Borowiec
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 252:252-255
Introduction Recurrent miscarriage is a serious clinical problem that affects 1–5 % of all couples trying to conceive. Although the incidence of Smith-Lemli-Opitz Syndrome (SLOS, OMIM #270400), an autosomal recessive condition caused by variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d09d957c75eaf1a3d0e82d214ab85e4e
https://doi.org/10.1016/j.ejogrb.2020.05.063
https://doi.org/10.1016/j.ejogrb.2020.05.063
Publikováno v:
Pediatria Polska. 93:343-348
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8baa97606d6524e5fc2062a0ac51116b
https://doi.org/10.5114/polp.2018.77747
https://doi.org/10.5114/polp.2018.77747
Autor:
Marta Kacprzak, Marta Chrzanowska, Maciej Borowiec, Hanna Moczulska, Piotr Sieroszewski, Beata Skoczylas
Publikováno v:
Ginekologia Polska. 87:722-726
Recurrent miscarriage is an important problem in reproductive health, which affects 1-5% of couples. The aim of this article is to summarize current knowledge on the genetic causes of recurrent miscarriage. It presents the most common parental geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93751bba4a221cd727d6c9ee188f5024
https://doi.org/10.5603/gp.2016.0075
https://doi.org/10.5603/gp.2016.0075
Autor:
Moczulska, Hanna, Pietrusinski, Michal, Serafin, Marcin, Skoczylas, Beata, Sieroszewski, Piotr, Borowiec, Maciej
Publikováno v:
Application of Clinical Genetics; Oct2022, Vol. 15, p145-151, 7p
Autor:
Šošić G. M.1 gordana.sosic.2011.02@gmail.com, Jović N.2,3, Rakić B.4, Dimitrijević A.2,5, Varjačić M.2,3
Publikováno v:
Balkan Journal of Medical Genetics. Dec2017, Vol. 20 Issue 2, p11-18. 8p.
Publikováno v:
Women's Health Weekly; 12/29/2023, p332-332, 1p