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Pavlos Fanis

Showing results (31-40 of 36) with videos related to

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Frontiers in Endocrinology|September 28, 2020
GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in <i>ANOS1, RNF216, WDR11, FGFR1, CHD7</i>, and <i>POLR3A</i> Genes in a Case Series and Review of the LiteratureVassos Neocleous, Pavlos Fanis, Meropi Toumba, et al.
Orphanet Journal of Rare Diseases|October 3, 2021
Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registryPanayiotis K Yiallouros, Andreas Μ Matthaiou, Pinelopi Anagnostopoulou, et al.
Haematologica|May 25, 2011
The DNA binding factor Hmg20b is a repressor of erythroid differentiationFatemehsadat Esteghamat, Thamar Bryn van Dijk, Harald Braun, et al.
Frontiers in Endocrinology|October 11, 2021
Pathogenic and Low-Frequency Variants in Children With Central Precocious PubertyVassos Neocleous, Pavlos Fanis, Meropi Toumba, et al.
Scientific Reports|May 21, 2016
The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective studyPetros Kountouris, Ioanna Kousiappa, Thessalia Papasavva, et al.
Nature Genetics|August 3, 2010
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobinJoseph Borg, Petros Papadopoulos, Marianthi Georgitsi, et al.
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Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Frontiers in Endocrinology|September 28, 2020
GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in <i>ANOS1, RNF216, WDR11, FGFR1, CHD7</i>, and <i>POLR3A</i> Genes in a Case Series and Review of the LiteratureVassos Neocleous, Pavlos Fanis, Meropi Toumba, et al.
Orphanet Journal of Rare Diseases|October 3, 2021
Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registryPanayiotis K Yiallouros, Andreas Μ Matthaiou, Pinelopi Anagnostopoulou, et al.
Haematologica|May 25, 2011
The DNA binding factor Hmg20b is a repressor of erythroid differentiationFatemehsadat Esteghamat, Thamar Bryn van Dijk, Harald Braun, et al.
Frontiers in Endocrinology|October 11, 2021
Pathogenic and Low-Frequency Variants in Children With Central Precocious PubertyVassos Neocleous, Pavlos Fanis, Meropi Toumba, et al.
Scientific Reports|May 21, 2016
The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective studyPetros Kountouris, Ioanna Kousiappa, Thessalia Papasavva, et al.
Nature Genetics|August 3, 2010
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobinJoseph Borg, Petros Papadopoulos, Marianthi Georgitsi, et al.
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