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X
Ayda Khalfallah
19  Ergebnisse:
Personensuche X
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1

ZEB2 haploinsufficient Mowat-Wilson syndrome induced plurip..:

Schuster, Jens ; Klar, Joakim ; Khalfallah, Ayda...
Frontiers in Molecular Neuroscience.  15 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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2

Mowat-Wilson syndrome: Generation of two human iPS cell lin..:

Schuster, Jens ; Sobol, Maria ; Fatima, Ambrin...
Stem Cell Research.  39 (2019)  - p. 101518 , 2019
Link: https://doi.org/10.1016/..
 
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3

Recurrent GATA1 mutations in Diamond‐Blackfan anaemia:

Klar, Joakim ; Khalfallah, Ayda ; Arzoo, Pakeeza Shaiq..
British Journal of Haematology.  166 (2014)  6 - p. 949-951 , 2014
Link: https://doi.org/10.1111/..
 
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4

COL1A1 association and otosclerosis: A meta‐analysis:

Schrauwen, Isabelle ; Khalfallah, Ayda ; Ealy, Megan...
American Journal of Medical Genetics Part A.  158A (2012)  5 - p. 1066-1070 , 2012
Link: https://doi.org/10.1002/..
 
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5

Association of COL1A1 and TGFB1 Polymorphisms with Otoscler..:

Khalfallah, Ayda ; Schrauwen, Isabelle ; Mnejja, Malek...
Annals of Human Genetics.  75 (2011)  5 - p. 598-604 , 2011
Link: https://doi.org/10.1111/..
 
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6

A novel missense mutation in the ESRRB gene causes DFNB35 h..:

Ben Saïd, Mariem ; Ayedi, Leila ; Mnejja, Melek...
European Journal of Medical Genetics.  54 (2011)  6 - p. e535-e541 , 2011
Link: https://doi.org/10.1016/..
 
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7

Genetic variants in RELN are associated with otosclerosis i..:

Khalfallah, Ayda ; Schrauwen, Isabelle ; Mnaja, Malek...
Annals of Human Genetics.  74 (2010)  5 - p. 399-405 , 2010
Link: https://doi.org/10.1111/..
 
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8

Table_1_ZEB2 haploinsufficient Mowat-Wilson syndrome induce..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
doi:10.3389/fnmol.2022.988993.s004.  , 2022
Link: https://doi.org/10.3389/..
 
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9

Table_4_ZEB2 haploinsufficient Mowat-Wilson syndrome induce..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
doi:10.3389/fnmol.2022.988993.s007.  , 2022
Link: https://doi.org/10.3389/..
 
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10

Image_1_ZEB2 haploinsufficient Mowat-Wilson syndrome induce..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
doi:10.3389/fnmol.2022.988993.s001.  , 2022
Link: https://doi.org/10.3389/..
 
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11

Image_2_ZEB2 haploinsufficient Mowat-Wilson syndrome induce..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
doi:10.3389/fnmol.2022.988993.s002.  , 2022
Link: https://doi.org/10.3389/..
 
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12

Table_2_ZEB2 haploinsufficient Mowat-Wilson syndrome induce..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
doi:10.3389/fnmol.2022.988993.s005.  , 2022
Link: https://doi.org/10.3389/..
 
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13

ZEB2 haploinsufficient Mowat-Wilson syndrome induced plurip..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
https://www.frontiersin.org/articles/10.3389/fnmol.2022.988993/full.  , 2022
Link: https://doi.org/10.3389/..
 
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14

Image_3_ZEB2 haploinsufficient Mowat-Wilson syndrome induce..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
doi:10.3389/fnmol.2022.988993.s003.  , 2022
Link: https://doi.org/10.3389/..
 
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15

Table_3_ZEB2 haploinsufficient Mowat-Wilson syndrome induce..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
doi:10.3389/fnmol.2022.988993.s006.  , 2022
Link: https://doi.org/10.3389/..
 
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