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Shiri, Amirmasoud
6  Ergebnisse:
Personensuche X
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1

Jaberi-Elahi syndrome: Exploring a novel GTPBP2 mutation an..:

Manoochehri, Jamal ; Shiri, Amirmasoud ; Khoddam, Somayeh...
European Journal of Medical Genetics.  70 (2024)  - p. 104953 , 2024
Link: https://doi.org/10.1016/..
 
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2

A Comprehensive Consolidation of Data on the Relationship b..:

Golshan-Tafti, Mohammad ; Dastgheib, Seyed Alireza ; Bahrami, Reza...
Journal of Stomatology, Oral and Maxillofacial Surgery.  , 2024
Link: https://doi.org/10.1016/..
 
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3

ST3GAL3 deficiency with autistic behavior: First descriptio..:

Manoochehri, Jamal ; Khamirani, Hossein Jafari ; Kamal, Neda...
Gene Reports.  35 (2024)  - p. 101892 , 2024
Link: https://doi.org/10.1016/..
 
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4

Two siblings with PEX11B-related peroxisome biogenesis diso..:

Khoddam, Somayeh ; Kamal, Neda ; Shiri, Amirmasoud...
European Journal of Medical Genetics.  68 (2024)  - p. 104928 , 2024
Link: https://doi.org/10.1016/..
 
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5

Comprehensive data on the relationship between KCNJ11 polym..:

Golshan-Tafti, Mohammad ; Bahrami, Reza ; Dastgheib, Seyed Alireza...
Journal of Diabetes & Metabolic Disorders.  23 (2024)  1 - p. 475-486 , 2024
Link: https://doi.org/10.1007/..
 
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6

Novel insight into the phenotype of microcephaly 19 in the ..:

Shiri, Amirmasoud ; Jafari Khamirani, Hossein ; Kamal, Neda...
European Journal of Medical Genetics.  66 (2023)  10 - p. 104846 , 2023
Link: https://doi.org/10.1016/..
 
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