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Eissa Faqeih

Showing results (1-10 of 88) with videos related to

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European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|November 4, 2015
Familial pseudotail, scoliosis and synpolydactyly syndromeMohammad Alfawareh, Tamer Orief, Eissa Faqeih
Neurogenetics|July 24, 2013
A truncating mutation in B3GNT1 causes severe Walker-Warburg syndromeRanad Shaheen, Eissa Faqeih, Shinu Ansari, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2Eissa Faqeih, Peter Roughley, Francis H Glorieux, et al.
Cardiology in the Young|November 7, 2013
Cardiac involvement in geleophysic dysplasia in three siblings of a Saudi familyMotea E Elhoury, Eissa Faqeih, Abdulrahman S Almoukirish, et al.
American Journal of Medical Genetics. Part A|August 1, 2007
Four siblings with distal renal tubular acidosis and nephrocalcinosis, neurobehavioral impairment, short stature, and distinctive facial appearance: a possible new autosomal recessive syndromeEissa Faqeih, Samhar I Al-Akash, Nadia Sakati, et al.
Nature Communications|May 20, 2020
DALRD3 encodes a protein mutated in epileptic encephalopathy that targets arginine tRNAs for 3-methylcytosine modificationJenna M Lentini, Hessa S Alsaif, Eissa Faqeih, et al.
Clinical Dysmorphology|June 11, 2008
Localized acalvaria with craniosynostosisEissa Faqeih, Zoltan Patay, Zuhair Rahbeeni, et al.
Frontiers in Medicine|November 29, 2023
Non-invasive prenatal testing: a revolutionary journey in prenatal testingMalak Abedalthagafi, Shahad Bawazeer, Romy I Fawaz, et al.
Human Molecular Genetics|July 25, 2014
ZBTB42 mutation defines a novel lethal congenital contracture syndrome (LCCS6)Nisha Patel, Laura L Smith, Eissa Faqeih, et al.
Human Genetics|April 9, 2016
A homozygous truncating mutation in PUS3 expands the role of tRNA modification in normal cognitionRanad Shaheen, Lu Han, Eissa Faqeih, et al.
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|November 4, 2015
Familial pseudotail, scoliosis and synpolydactyly syndromeMohammad Alfawareh, Tamer Orief, Eissa Faqeih
Neurogenetics|July 24, 2013
A truncating mutation in B3GNT1 causes severe Walker-Warburg syndromeRanad Shaheen, Eissa Faqeih, Shinu Ansari, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2Eissa Faqeih, Peter Roughley, Francis H Glorieux, et al.
Cardiology in the Young|November 7, 2013
Cardiac involvement in geleophysic dysplasia in three siblings of a Saudi familyMotea E Elhoury, Eissa Faqeih, Abdulrahman S Almoukirish, et al.
American Journal of Medical Genetics. Part A|August 1, 2007
Four siblings with distal renal tubular acidosis and nephrocalcinosis, neurobehavioral impairment, short stature, and distinctive facial appearance: a possible new autosomal recessive syndromeEissa Faqeih, Samhar I Al-Akash, Nadia Sakati, et al.
Nature Communications|May 20, 2020
DALRD3 encodes a protein mutated in epileptic encephalopathy that targets arginine tRNAs for 3-methylcytosine modificationJenna M Lentini, Hessa S Alsaif, Eissa Faqeih, et al.
Clinical Dysmorphology|June 11, 2008
Localized acalvaria with craniosynostosisEissa Faqeih, Zoltan Patay, Zuhair Rahbeeni, et al.
Frontiers in Medicine|November 29, 2023
Non-invasive prenatal testing: a revolutionary journey in prenatal testingMalak Abedalthagafi, Shahad Bawazeer, Romy I Fawaz, et al.
Human Molecular Genetics|July 25, 2014
ZBTB42 mutation defines a novel lethal congenital contracture syndrome (LCCS6)Nisha Patel, Laura L Smith, Eissa Faqeih, et al.
Human Genetics|April 9, 2016
A homozygous truncating mutation in PUS3 expands the role of tRNA modification in normal cognitionRanad Shaheen, Lu Han, Eissa Faqeih, et al.
Pageof 9