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
Shohat, Mordechai
171
results:
Online X
Search for persons
X
Format
Online (171)
Mediatypes
Articles (Online) (127)
OpenAccess-fulltext (44)
Sorted by: Relevance
Sorted by: Year
?
1
A de novo pathogenic variant in DHX30 gene in a fetus with ..:
Haratz, Karina Krajden
;
Malinger, Gustavo
;
Erlik, Uri
...
Prenatal Diagnosis. 44 (2024) 3 - p. 357-359 , 2024
Link:
https://doi.org/10.1002/..
?
2
1063 Prenatal Exome in low-risk pregnancies and apparently ..:
Levy, Michal
;
Lifshitz, Shira
;
Goldenberg-Fumanov, Mirela
...
American Journal of Obstetrics and Gynecology. 230 (2024) 1 - p. S558-S559 , 2024
Link:
https://doi.org/10.1016/..
?
3
Exome sequencing in every pregnancy? Results of trio exome ..:
Levy, Michal
;
Lifshitz, Shira
;
Goldenberg‐Fumanov, Mirela
...
Prenatal Diagnosis. , 2024
Link:
https://doi.org/10.1002/..
?
4
Exploring inheritance, and clinical penetrance of distal Xq..:
Levy, Michal
;
Elron, Eyal
;
Shohat, Mordechai
...
Journal of Human Genetics. 69 (2024) 7 - p. 337-343 , 2024
Link:
https://doi.org/10.1038/..
?
5
Proximal 1q21 duplication: A syndrome or a susceptibility l..:
Levy, Michal
;
Shohat, Mordechai
;
Kahana, Sarit
...
American Journal of Medical Genetics Part A. 191 (2023) 10 - p. 2551-2557 , 2023
Link:
https://doi.org/10.1002/..
?
6
Whole exome germline sequencing in early‐onset prostate can..:
Siegelmann‐Danieli, Nava
;
Neiman, Victoria
;
Bareket‐Samish, Avital
...
The Prostate. 84 (2023) 1 - p. 39-46 , 2023
Link:
https://doi.org/10.1002/..
?
7
A beneficial role of GLP-1 receptor agonist therapy in ABCC..:
Nakhleh, Afif
;
Goldenberg-Furmanov, Mirela
;
Goldstein, Rayna
..
Journal of Diabetes and its Complications. 37 (2023) 9 - p. 108566 , 2023
Link:
https://doi.org/10.1016/..
?
8
Bi-allelic variants in INTS11 are associated with a complex..:
Tepe, Burak
;
Macke, Erica L.
;
Niceta, Marcello
...
The American Journal of Human Genetics. 110 (2023) 5 - p. 774-789 , 2023
Link:
https://doi.org/10.1016/..
?
9
Autosomal dominant non-syndromic hearing loss maps to DFNA3..:
Pater, Justin A.
;
Penney, Cindy
;
O'Rielly, Darren D.
...
Human Genetics. 141 (2022) 3-4 - p. 431-444 , 2022
Link:
https://doi.org/10.1007/..
?
10
Prenatal diagnosis of microcephaly as shown by plateauing o..:
Malinger, Gustavo
;
Haratz Krajden, Karina
;
Brinbaum, Roee
...
Prenatal Diagnosis. 42 (2022) 10 - p. 1343-1345 , 2022
Link:
https://doi.org/10.1002/..
?
11
Refining the Phenotypic Spectrum of KMT5B-Associated Develo..:
Eliyahu, Aviva
;
Barel, Ortal
;
Greenbaum, Lior
...
Frontiers in Pediatrics. 10 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
12
Benefit versus risk of chromosomal microarray analysis perf..:
Moshonov, Rami
;
Hod, Keren
;
Azaria, Bella
...
PLOS ONE. 16 (2021) 4 - p. e0250734 , 2021
Link:
https://doi.org/10.1371/..
?
13
Early and late manifestations of neuropathy due to HSPB1 mu..:
Greenbaum, Lior
;
Ben‐David, Merav
;
Nikitin, Vera
...
Annals of Clinical and Translational Neurology. 8 (2021) 6 - p. 1260-1268 , 2021
Link:
https://doi.org/10.1002/..
?
14
High rate of abnormal findings in Prenatal Exome Trio in lo..:
Vaknin, Noam
;
Azoulay, Noy
;
Tsur, Erez
...
Prenatal Diagnosis. 42 (2021) 6 - p. 725-735 , 2021
Link:
https://doi.org/10.1002/..
?
15
Biallelic variants in ETV2 in a family with congenital hear..:
Basel-Salmon, Lina
;
Ruhrman-Shahar, Noa
;
Barel, Ortal
...
European Journal of Medical Genetics. 64 (2021) 2 - p. 104124 , 2021
Link:
https://doi.org/10.1016/..
1-15