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Almoallem, Basamat
17
results:
Search for persons
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Format
Online (17)
Mediatypes
Articles (Online) (8)
OpenAccess-fulltext (9)
Sorted by: Relevance
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?
1
Autozygome‐guided exome‐first study in a consanguineous coh..:
Del Pozo‐Valero, Marta
;
Almoallem, Basamat
;
Dueñas Rey, Alfredo
...
Clinical Genetics. 106 (2024) 2 - p. 127-139 , 2024
Link:
https://doi.org/10.1111/..
?
2
Novel biallelic AHR splice site mutation cause isolated fov..:
Almoallem, Basamat
Acta Ophthalmologica. 100 (2022) S275 - p. , 2022
Link:
https://doi.org/10.1111/..
?
3
Novel phenotype–genotype correlation with PEX6 gene in Saud..:
Almoallem, Basamat
Acta Ophthalmologica. 100 (2022) S275 - p. , 2022
Link:
https://doi.org/10.1111/..
?
4
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
The American Journal of Human Genetics. 106 (2020) 6 - p. 859-871 , 2020
Link:
https://doi.org/10.1016/..
?
5
The majority of autosomal recessive nanophthalmos and poste..:
Almoallem, Basamat
;
Arno, Gavin
;
De Zaeytijd, Julie
...
Scientific Reports. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
6
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
The American Journal of Human Genetics. 107 (2020) 3 - p. 580 , 2020
Link:
https://doi.org/10.1016/..
?
7
Oculocerebrocutaneous syndrome (Delleman Oorthuys syndrome)..:
Jamjoom, Hanan
;
Osman, Mohamed
;
AlMoallem, Basamat
.
European Journal of Ophthalmology. 32 (2020) 1 - p. NP66-NP70 , 2020
Link:
https://doi.org/10.1177/..
?
8
Homozygous stop mutation in AHR causes autosomal recessive ..:
Mayer, Anja K
;
Mahajnah, Muhammad
;
Thomas, Mervyn G
...
Brain. 142 (2019) 6 - p. 1528-1534 , 2019
Link:
https://doi.org/10.1093/..
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9
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2020.04.018. , 2020
Link:
https://hal.science/hal-..
?
10
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2020.04.018. , 2020
Link:
https://hal.science/hal-..
?
11
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273530/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
12
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477002/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
13
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2020.04.018. , 2020
Link:
https://hal.science/hal-..
?
14
The majority of autosomal recessive nanophthalmos and poste..:
Almoallem, Basamat
;
Arno, Gavin
;
De Zaeytijd, Julie
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987234/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
15
The majority of autosomal recessive nanophthalmos and poste..:
Almoallem, Basamat
;
Arno, Gavin
;
De Zaeytijd, Julie
...
qt9rm8d2d9. , 2020
Link:
https://escholarship.org..
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