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Hanan Hamamy

Showing results (31-40 of 56) with videos related to

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Bone|September 3, 2014
Exome sequencing reveals a mutation in DMP1 in a family with familial sclerosing bone dysplasiaMarie-Hélène Gannagé-Yared, Periklis Makrythanasis, Eliane Chouery, et al.
Human Resources for Health|December 9, 2016
E-learning for research capacity strengthening in sexual and reproductive health: the experience of the Geneva Foundation for Medical Education and Research and the Department of Reproductive Health and Research, World Health OrganizationKarim Abawi, Venkatraman Chandra-Mouli, Igor Toskin, et al.
Nature Genetics|May 15, 2012
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Carine Bonnard, Anna C Strobl, Mohammad Shboul, et al.
Bone Reports|July 26, 2016
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralizationCorey J Cain, Nathalie Gaborit, Wint Lwin, et al.
European Journal of Human Genetics : EJHG|February 18, 2011
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disordersJana Herholz, Alessandra Meloni, Mara Marongiu, et al.
Stem Cell Research|December 20, 2021
Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 systemRobin Canac, Amandine Caillaud, Bastien Cimarosti, et al.
American Journal of Human Genetics|December 7, 2010
Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signalingJing Tian, Ling Ling, Mohammad Shboul, et al.
Hemoglobin|June 13, 2012
Sickle cell disease in the Kurdish population of northern IraqNasir A S Al-Allawi, Sana D Jalal, Farida F Nerwey, et al.
Public Health Genomics|January 24, 2015
Premarital screening for hemoglobinopathies: experience of a single center in Kurdistan, IraqNasir A S Al-Allawi, Adnan A S Al-Doski, Raji S D Markous, et al.
Journal of Community Genetics|April 9, 2011
Community genetics. Its definition 2010Leo P Ten Kate, Lihadh Al-Gazali, Sonia Anand, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Bone|September 3, 2014
Exome sequencing reveals a mutation in DMP1 in a family with familial sclerosing bone dysplasiaMarie-Hélène Gannagé-Yared, Periklis Makrythanasis, Eliane Chouery, et al.
Human Resources for Health|December 9, 2016
E-learning for research capacity strengthening in sexual and reproductive health: the experience of the Geneva Foundation for Medical Education and Research and the Department of Reproductive Health and Research, World Health OrganizationKarim Abawi, Venkatraman Chandra-Mouli, Igor Toskin, et al.
Nature Genetics|May 15, 2012
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Carine Bonnard, Anna C Strobl, Mohammad Shboul, et al.
Bone Reports|July 26, 2016
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralizationCorey J Cain, Nathalie Gaborit, Wint Lwin, et al.
European Journal of Human Genetics : EJHG|February 18, 2011
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disordersJana Herholz, Alessandra Meloni, Mara Marongiu, et al.
Stem Cell Research|December 20, 2021
Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 systemRobin Canac, Amandine Caillaud, Bastien Cimarosti, et al.
American Journal of Human Genetics|December 7, 2010
Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signalingJing Tian, Ling Ling, Mohammad Shboul, et al.
Hemoglobin|June 13, 2012
Sickle cell disease in the Kurdish population of northern IraqNasir A S Al-Allawi, Sana D Jalal, Farida F Nerwey, et al.
Public Health Genomics|January 24, 2015
Premarital screening for hemoglobinopathies: experience of a single center in Kurdistan, IraqNasir A S Al-Allawi, Adnan A S Al-Doski, Raji S D Markous, et al.
Journal of Community Genetics|April 9, 2011
Community genetics. Its definition 2010Leo P Ten Kate, Lihadh Al-Gazali, Sonia Anand, et al.
Pageof 6