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Hanan Hamamy

Showing results (21-30 of 56) with videos related to

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BMC Blood Disorders|July 7, 2010
Prevalence and molecular characterization of Glucose-6-Phosphate dehydrogenase deficient variants among the Kurdish population of Northern IraqNasir Al-Allawi, Adil A Eissa, Jaladet Ms Jubrael, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 18, 2015
Triple A syndrome with a novel indel mutation in the AAAS gene and delayed pubertyHaidar Bustanji, Bashar Sahar, Angela Huebner, et al.
Human Mutation|May 28, 2014
A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis, hearing impairment, camptodactyly, and arachnodactylyPeriklis Makrythanasis, Samia Temtamy, Mona S Aglan, et al.
Seizure|September 13, 2015
Familial epilepsy in Algeria: Clinical features and inheritance profilesAmina Chentouf, Aïcha Dahdouh, Michel Guipponi, et al.
Journal of Medical Screening|October 23, 2013
The first five years of a preventive programme for haemoglobinopathies in Northeastern IraqNasir A S Al-Allawi, Sana D Jalal, Najmaddin H Ahmed, et al.
Journal of Community Genetics|August 16, 2018
Rare single gene disorders: estimating baseline prevalence and outcomes worldwideHannah Blencowe, Sowmiya Moorthie, Mary Petrou, et al.
Journal of Child Neurology|April 12, 2008
Griscelli syndrome type 2: a rare and lethal disorderAmira Masri, Faris G Bakri, Maissa Al-Hussaini, et al.
Clinical Neurology and Neurosurgery|December 17, 2019
Congenital insensitivity to pain with anhidrosis syndrome: A series from JordanAmira Masri, Mohammad Shboul, Aisha Khasawneh, et al.
BMC Blood Disorders|March 29, 2012
Molecular characterization of glucose-6-phosphate dehydrogenase deficient variants in Baghdad city - IraqBassam Ms Al-Musawi, Nasir Al-Allawi, Ban A Abdul-Majeed, et al.
Human Genomics|July 17, 2016
Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreePeriklis Makrythanasis, Michel Guipponi, Federico A Santoni, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
BMC Blood Disorders|July 7, 2010
Prevalence and molecular characterization of Glucose-6-Phosphate dehydrogenase deficient variants among the Kurdish population of Northern IraqNasir Al-Allawi, Adil A Eissa, Jaladet Ms Jubrael, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 18, 2015
Triple A syndrome with a novel indel mutation in the AAAS gene and delayed pubertyHaidar Bustanji, Bashar Sahar, Angela Huebner, et al.
Human Mutation|May 28, 2014
A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis, hearing impairment, camptodactyly, and arachnodactylyPeriklis Makrythanasis, Samia Temtamy, Mona S Aglan, et al.
Seizure|September 13, 2015
Familial epilepsy in Algeria: Clinical features and inheritance profilesAmina Chentouf, Aïcha Dahdouh, Michel Guipponi, et al.
Journal of Medical Screening|October 23, 2013
The first five years of a preventive programme for haemoglobinopathies in Northeastern IraqNasir A S Al-Allawi, Sana D Jalal, Najmaddin H Ahmed, et al.
Journal of Community Genetics|August 16, 2018
Rare single gene disorders: estimating baseline prevalence and outcomes worldwideHannah Blencowe, Sowmiya Moorthie, Mary Petrou, et al.
Journal of Child Neurology|April 12, 2008
Griscelli syndrome type 2: a rare and lethal disorderAmira Masri, Faris G Bakri, Maissa Al-Hussaini, et al.
Clinical Neurology and Neurosurgery|December 17, 2019
Congenital insensitivity to pain with anhidrosis syndrome: A series from JordanAmira Masri, Mohammad Shboul, Aisha Khasawneh, et al.
BMC Blood Disorders|March 29, 2012
Molecular characterization of glucose-6-phosphate dehydrogenase deficient variants in Baghdad city - IraqBassam Ms Al-Musawi, Nasir Al-Allawi, Ban A Abdul-Majeed, et al.
Human Genomics|July 17, 2016
Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreePeriklis Makrythanasis, Michel Guipponi, Federico A Santoni, et al.
Pageof 6