I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Elhossini, Rasha Moheb
13
results:
Search for persons
X
Sorted by: Relevance
Sorted by: Year
?
1
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/..
?
2
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/..
?
3
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/..
?
4
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/..
?
5
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/..
?
6
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/..
?
7
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/..
?
8
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/..
?
9
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/..
?
10
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/..
?
11
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/..
?
12
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/..
?
13
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/..
1-13