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Hijazi, Hadia
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1

P623: Cytogenetic findings in a clinical next generation se..:

Hijazi, Hadia ; Luke, Tamara ; Pechter, Kieran...
Genetics in Medicine Open.  2 (2024)  - p. 101529 , 2024
Link: https://doi.org/10.1016/..
 
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2

Developmental genomics of limb malformations: Allelic serie..:

Duan, Ruizhi ; Hijazi, Hadia ; Gulec, Elif Yilmaz...
Human Genetics and Genomics Advances.  3 (2022)  4 - p. 100132 , 2022
Link: https://doi.org/10.1016/..
 
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3

Neurobehavioral phenotype of Kabuki syndrome: Anxiety is a ..:

Kalinousky, Allison J. ; Rapp, Tyler ; Hijazi, Hadia...
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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4

Inside Back Cover, Volume 41, Issue 1:

Hijazi, Hadia ; Coelho, Fernanda S. ; Gonzaga‐Jauregui, Claudia...
Human Mutation.  41 (2019)  1 - p. , 2019
Link: https://doi.org/10.1002/..
 
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5

Interchromosomal template-switching as a novel molecular me..:

Baylor-Hopkins Center for Mendelian Genomics ; Carvalho, Claudia M. B. ; Coban-Akdemir, Zeynep...
Genome Medicine.  11 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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6

Exome Sequencing of a Primary Ovarian Insufficiency Cohort ..:

Jolly, Angad ; Bayram, Yavuz ; Turan, Serap...
The Journal of Clinical Endocrinology & Metabolism.  104 (2019)  8 - p. 3049-3067 , 2019
Link: https://doi.org/10.1210/..
 
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7

Xq22 deletions and correlation with distinct neurological d..:

Hijazi, Hadia ; Coelho, Fernanda S. ; Gonzaga‐Jauregui, Claudia...
Human Mutation.  41 (2019)  1 - p. 150-168 , 2019
Link: https://doi.org/10.1002/..
 
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8

Distinct patterns of complex rearrangements and a mutationa..:

Bahrambeigi, Vahid ; Song, Xiaofei ; Sperle, Karen...
Genome Medicine.  11 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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9

Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle..:

Trivellin, Giampaolo ; Sharwood, Erin ; Hijazi, Hadia...
Journal of the Endocrine Society.  2 (2018)  10 - p. 1100-1108 , 2018
Link: https://doi.org/10.1210/..
 
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10

ARL6IP6, a susceptibility locus for ischemic stroke, is mut..:

Abumansour, Iman S. ; Hijazi, Hadia ; Alazmi, Anas...
Human Genetics.  134 (2015)  8 - p. 815-822 , 2015
Link: https://doi.org/10.1007/..
 
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11

TLE6 mutation causes the earliest known human embryonic let..:

Alazami, Anas M. ; Awad, Salma M. ; Coskun, Serdar...
Genome Biology.  16 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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12

Accelerating Novel Candidate Gene Discovery in Neurogenetic..:

Alazami, Anas M. ; Patel, Nisha ; Shamseldin, Hanan E....
Cell Reports.  10 (2015)  2 - p. 148-161 , 2015
Link: https://doi.org/10.1016/..
 
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13

Pellagra-Like Syndrome Proves to Be a Variant of Xeroderma ..:

Salih, Mustafa ; Hijazi, Hadia ; Hamad, Muddathir...
Neurology.  82 (2014)  10_supplement - p. , 2014
Link: https://doi.org/10.1212/..
 
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14

Mutations in LRPAP1 Are Associated with Severe Myopia in Hu..:

Aldahmesh, Mohammed A. ; Khan, Arif O. ; Alkuraya, Hisham...
The American Journal of Human Genetics.  93 (2013)  2 - p. 313-320 , 2013
Link: https://doi.org/10.1016/..
 
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15

CYP1B1 analysis of unilateral primary newborn glaucoma in S..:

Khan, Arif O. ; Aldahmesh, Mohammed A. ; Mohamed, Jawahir Y...
Journal of American Association for Pediatric Ophthalmology and Strabismus.  16 (2012)  6 - p. 571-572 , 2012
Link: https://doi.org/10.1016/..
 
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