Kaygusuz, Emrah, Khayyat, Arwa Ishaq A., Abdullah, Uzma, Budde, Birgit Susanne, Asif, Maria, Ahmed, Ilyas, Makhdoom, Ehtisham Ul Haq, Sur-Erdem, Ilknur, Baig, Jamshaid Mahmood, Khan, Muhammad Mohsin Ali, Toliat, Mohammad Reza, Becker, Christian, Anwar, Haseeb, Iqbal, Maria, Fischer, Sarah, Jameel, Muhammad, Sher, Muhammad, Tariq, Muhammad, Malik, Naveed Altaf, Noegel, Angelika A., Hassan, Muhammad Jawad, Thiele, Holger, Tinschert, Sigrid, Eichinger, Ludwig, Honing, Stefan, Baig, Shahid Mahmood, Nurnberg, Peter and Hussain, Muhammad Sajid
(2022).
A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome (vol 100, pg 486, 2021).
Clin. Genet., 101 (2).
S. 272 - 273.
HOBOKEN:
WILEY.
ISSN 1399-0004
Full text not available from this repository.
Item Type: |
Journal Article
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Creators: |
Creators | Email | ORCID | ORCID Put Code |
---|
Kaygusuz, Emrah | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Khayyat, Arwa Ishaq A. | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Abdullah, Uzma | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Budde, Birgit Susanne | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Asif, Maria | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Ahmed, Ilyas | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Makhdoom, Ehtisham Ul Haq | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Sur-Erdem, Ilknur | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Baig, Jamshaid Mahmood | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Khan, Muhammad Mohsin Ali | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Toliat, Mohammad Reza | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Becker, Christian | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Anwar, Haseeb | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Iqbal, Maria | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Fischer, Sarah | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Jameel, Muhammad | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Sher, Muhammad | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Tariq, Muhammad | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Malik, Naveed Altaf | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Noegel, Angelika A. | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Hassan, Muhammad Jawad | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Thiele, Holger | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Tinschert, Sigrid | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Eichinger, Ludwig | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Honing, Stefan | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Baig, Shahid Mahmood | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Nurnberg, Peter | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED | Hussain, Muhammad Sajid | UNSPECIFIED | UNSPECIFIED | UNSPECIFIED |
|
URN: |
urn:nbn:de:hbz:38-692872 |
DOI: |
10.1111/cge.14092 |
Journal or Publication Title: |
Clin. Genet. |
Volume: |
101 |
Number: |
2 |
Page Range: |
S. 272 - 273 |
Date: |
2022 |
Publisher: |
WILEY |
Place of Publication: |
HOBOKEN |
ISSN: |
1399-0004 |
Language: |
English |
Faculty: |
Unspecified |
Divisions: |
Unspecified |
Subjects: |
no entry |
Uncontrolled Keywords: |
Keywords | Language |
---|
Genetics & Heredity | Multiple languages |
|
URI: |
http://kups.ub.uni-koeln.de/id/eprint/69287 |
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