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Elhossini, Rasha M.
16  results:
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1

Brachyolmia, dental anomalies and short stature (DASS): Phe..:

Nawaz, Hamed ; Parveen, Asia ; Khan, Sher Alam...
Heliyon.  10 (2024)  1 - p. e23688 , 2024
Link: https://doi.org/10.1016/..
 
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2

The Diagnostic Value of Whole-Exome Sequencing in a Spectru..:

Ashaat, Engy A. ; Ahmed, Hoda A. ; Elaraby, Nesma M....
Molecular Neurobiology.  61 (2023)  8 - p. 4949-4961 , 2023
Link: https://doi.org/10.1007/..
 
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3

CHST3‐related skeletal dysplasia in 14 patients: Identifica..:

Otaify, Ghada A. ; Elhossini, Rasha M. ; Abdel‐Ghafar, Sherif F....
American Journal of Medical Genetics Part A.  191 (2023)  8 - p. 2100-2112 , 2023
Link: https://doi.org/10.1002/..
 
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4

A recurrent KCNK4 variant in a dominant pedigree with hyper..:

Elhossini, Rasha M. ; Sayed, Inas M. ; Hellal, Usama Saad...
American Journal of Medical Genetics Part A.  194 (2023)  1 - p. 39-45 , 2023
Link: https://doi.org/10.1002/..
 
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5

Spondyloenchondrodysplasia in five new patients: identifica..:

Elhossini, Rasha M. ; Elbendary, Hasnaa M. ; Rafat, Karima..
Molecular Genetics and Genomics.  298 (2023)  3 - p. 709-720 , 2023
Link: https://doi.org/10.1007/..
 
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6

Bruck syndrome in 13 new patients: Identification of five n..:

Otaify, Ghada A. ; Abdel‐Hamid, Mohamed S. ; Hassib, Nehal F....
American Journal of Medical Genetics Part A.  188 (2022)  6 - p. 1815-1825 , 2022
Link: https://doi.org/10.1002/..
 
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7

Osteoporosis-pseudoglioma syndrome in four new patients: id..:

Abdel-Hamid, Mohamed S. ; Elhossini, Rasha M. ; Otaify, Ghada A...
Osteoporosis International.  33 (2022)  7 - p. 1501-1510 , 2022
Link: https://doi.org/10.1007/..
 
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8

A novel variant in GNPNAT1 gene causing a spondylo‐epi‐meta..:

Elhossini, Rasha Moheb ; Ahmed, Hoda Abdalla ; Otaify, Ghada...
American Journal of Medical Genetics Part A.  188 (2022)  10 - p. 2861-2868 , 2022
Link: https://doi.org/10.1002/..
 
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9

Novel LSS variants in alopecia and intellectual disability ..:

Elbendary, Hasnaa M. ; Marafi, Dana ; Saad, Ahmed K....
Clinical Genetics.  104 (2023)  3 - p. 344-349 , 2023
Link: https://doi.org/10.1111/..
 
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10

Expansion of the phenotypic and mutational spectrum of Carp..:

Khairat, Rabab ; Elhossini, Rasha ; Sobreira, Nara...
European Journal of Medical Genetics.  65 (2022)  1 - p. 104377 , 2022
Link: https://doi.org/10.1016/..
 
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11

Two new patients with focal dermal hypoplasia: A novel PORC..:

Elhossini, Rasha Moheb ; Abdel‐Hamid, Mohamed S. ; Ashaat, Engy...
Congenital Anomalies.  62 (2022)  2 - p. 68-77 , 2022
Link: https://doi.org/10.1111/..
 
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12

Variant characterisation and clinical profile in a large co..:

Altunoglu, Umut ; Palencia-Campos, Adrian ; Güneş, Nilay...
Journal of Medical Genetics.  61 (2024)  7 - p. 633-644 , 2024
Link: https://doi.org/10.1136/..
 
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13

Mutations in SCNM1 cause orofaciodigital syndrome due to mi..:

Iturrate, Asier ; Rivera-Barahona, Ana ; Flores, Carmen-Lisset...
The American Journal of Human Genetics.  109 (2022)  10 - p. 1828-1849 , 2022
Link: https://doi.org/10.1016/..
 
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14

Effect of Lycra Extension Percent on Single Jersey Knitted ..:

Sadek, R. ; El-Hossini, A. M. ; Eldeeb, A. S..
Journal of Engineered Fibers and Fabrics.  7 (2012)  2 - p. 155892501200700 , 2012
Link: https://doi.org/10.1177/..
 
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15

Aggrecan-related bone disorders; a novel heterozygous ACAN ..:

Ahmed, Hoda A. ; Elhossini, R. ; Aglan, M..
Journal of Genetic Engineering and Biotechnology.  22 (2024)  1 - p. 100341 , 2024
Link: https://doi.org/10.1016/..
 
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