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Rafiullah Rafiullah

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Human Genetics|December 2, 2021
Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypesMohamed H Al-Hamed, Wesam Kurdi, Rubina Khan, et al.
Cell Death & Disease|May 30, 2024
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformationsElizabeth A Werren, Emily R Peirent, Henna Jantti, et al.
American Journal of Human Genetics|October 5, 2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous PopulationDorota Monies, Mohammed Abouelhoda, Mirna Assoum, et al.
American Journal of Human Genetics|May 28, 2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous PopulationDorota Monies, Mohammed Abouelhoda, Mirna Assoum, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Human Genetics|December 2, 2021
Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypesMohamed H Al-Hamed, Wesam Kurdi, Rubina Khan, et al.
Cell Death & Disease|May 30, 2024
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformationsElizabeth A Werren, Emily R Peirent, Henna Jantti, et al.
American Journal of Human Genetics|October 5, 2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous PopulationDorota Monies, Mohammed Abouelhoda, Mirna Assoum, et al.
American Journal of Human Genetics|May 28, 2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous PopulationDorota Monies, Mohammed Abouelhoda, Mirna Assoum, et al.
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