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Yasser Sabr

Showing results (51-60 of 55) with videos related to

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European Journal of Human Genetics : EJHG|June 24, 2020
Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging featuresMarcello Scala, Geok Lin Chua, Cheen Fei Chin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 8, 2022
The morbid genome of ciliopathies: an updateHanan E Shamseldin, Ranad Shaheen, Nour Ewida, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2020
The morbid genome of ciliopathies: an updateHanan E Shamseldin, Ranad Shaheen, Nour Ewida, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2018
Expanding the phenome and variome of skeletal dysplasiaSateesh Maddirevula, Saud Alsahli, Lamees Alhabeeb, et al.
Human Genetics|June 11, 2017
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomesDorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, et al.
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Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
European Journal of Human Genetics : EJHG|June 24, 2020
Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging featuresMarcello Scala, Geok Lin Chua, Cheen Fei Chin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 8, 2022
The morbid genome of ciliopathies: an updateHanan E Shamseldin, Ranad Shaheen, Nour Ewida, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2020
The morbid genome of ciliopathies: an updateHanan E Shamseldin, Ranad Shaheen, Nour Ewida, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2018
Expanding the phenome and variome of skeletal dysplasiaSateesh Maddirevula, Saud Alsahli, Lamees Alhabeeb, et al.
Human Genetics|June 11, 2017
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomesDorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, et al.
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