Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Atefeh Hasanzadeh"'
Autor:
Asuman Koparir, Caroline Lekszas, Kemal Keseroglu, Thalia Rose, Lena Rappl, Aboulfazl Rad, Reza Maroofian, Nakul Narendran, Atefeh Hasanzadeh, Ehsan Ghayoor Karimiani, Felix Boschann, Uwe Kornak, Eva Klopocki, Ertuğrul M. Özbudak, Barbara Vona, Thomas Haaf, Daniel Liedtke
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-13 (2024)
Abstract Background/Objectives Rare genetic disorders causing specific congenital developmental abnormalities often manifest in single families. Investigation of disease-causing molecular features are most times lacking, although these investigations
Externí odkaz:
https://doaj.org/article/4ca8372a9ecd42798f65bafe5883ded4
Autor:
Julia Doll, Susanne Kolb, Linda Schnapp, Aboulfazl Rad, Franz Rüschendorf, Imran Khan, Abolfazl Adli, Atefeh Hasanzadeh, Daniel Liedtke, Sabine Knaup, Michaela AH Hofrichter, Tobias Müller, Marcus Dittrich, Il-Keun Kong, Hyung-Goo Kim, Thomas Haaf, Barbara Vona
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 1, p 311 (2020)
CDC14A encodes the Cell Division Cycle 14A protein and has been associated with autosomal recessive non-syndromic hearing loss (DFNB32), as well as hearing impairment and infertile male syndrome (HIIMS) since 2016. To date, only nine variants have be
Externí odkaz:
https://doaj.org/article/cebe6966194d47e88cac466d1e13fb4c
Autor:
Linda Schnapp, Barbara Vona, Thomas Haaf, Imran Khan, Tobias Müller, Franz Rüschendorf, Hyung-Goo Kim, Sabine Knaup, Abolfazl Adli, Michaela A.H. Hofrichter, Daniel Liedtke, Aboulfazl Rad, Susanne M. Kolb, Atefeh Hasanzadeh, Marcus Dittrich, Julia Doll, Il-Keun Kong
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 1
International Journal of Molecular Sciences, Vol 21, Iss 1, p 311 (2020)
Volume 21
Issue 1
International Journal of Molecular Sciences, Vol 21, Iss 1, p 311 (2020)
CDC14A encodes the Cell Division Cycle 14A protein and has been associated with autosomal recessive non-syndromic hearing loss (DFNB32), as well as hearing impairment and infertile male syndrome (HIIMS) since 2016. To date, only nine variants have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2386013fc9bcb1fededf0c67ed310e71
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/28514
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/28514
Autor:
Julia, Doll, Susanne, Kolb, Linda, Schnapp, Aboulfazl, Rad, Franz, Rüschendorf, Imran, Khan, Abolfazl, Adli, Atefeh, Hasanzadeh, Daniel, Liedtke, Sabine, Knaup, Michaela Ah, Hofrichter, Tobias, Müller, Marcus, Dittrich, Il-Keun, Kong, Hyung-Goo, Kim, Thomas, Haaf, Barbara, Vona
Publikováno v:
International Journal of Molecular Sciences
CDC14A encodes the Cell Division Cycle 14A protein and has been associated with autosomal recessive non-syndromic hearing loss (DFNB32), as well as hearing impairment and infertile male syndrome (HIIMS) since 2016. To date, only nine variants have be
Publikováno v:
International journal of rheumatic diseases. 21(1)
Background and aim Comparison between the effect of sonographic guided and blind knee injection of hyaluronic acid has been evaluated in this study. Methods and materials Sixty-one patients with primary knee osteoarthritis were randomly allocated int