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Kundishora, AJ
5  Ergebnisse:
Personensuche X
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1

Genomic approaches to improve the clinical diagnosis and ma..:

Allington, G ; Duy, PQ ; Ryou, J...
https://discovery.ucl.ac.uk/id/eprint/10142959/7/JNS_Revision_Final.docx.  , 2022
Link: https://discovery.ucl.ac..
 
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2

Rare pathogenic variants in WNK3 cause X-linked intellectua..:

Küry, S ; Zhang, J ; Besnard, T...
https://discovery.ucl.ac.uk/id/eprint/10151159/2/Shozeb_Rare%20pathogenic%20variants%20in%20WNK3%20cause%20X-linked%20intellectual%20disability_AAM.pdf.  , 2022
Link: https://discovery.ucl.ac..
 
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3

DIAPH1 Variants in Non-East Asian Patients With Sporadic Mo..:

Kundishora, AJ ; Peters, ST ; Pinard, A...
https://discovery.ucl.ac.uk/id/eprint/10130640/.  , 2021
Link: https://discovery.ucl.ac..
 
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4

Exome Sequencing Implicates Impaired GABA Signaling and Neu..:

Dong, W ; Jin, SC ; Allocco, A...
https://discovery.ucl.ac.uk/id/eprint/10112758/1/1-s2.0-S2589004220307446-main.pdf.  , 2020
Link: https://discovery.ucl.ac..
 
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5

Exome sequencing implicates genetic disruption of prenatal ..:

Jin, SC ; Dong, W ; Kundishora, AJ...
https://discovery.ucl.ac.uk/id/eprint/10113597/1/258248_0_art_file_4643678_q5x551_convrt.pdf.  , 2020
Link: https://discovery.ucl.ac..
 
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