Kumar, Runjun D
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4

The germline p53 activation syndrome: A new patient further..:

Kumar, Runjun D. ; Tosur, Mustafa ; Lalani, Seema R...
American Journal of Medical Genetics Part A.  188 (2022)  7 - p. 2204-2208 , 2022
 
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Clinical exome sequencing uncovers a high frequency of Mend..:

Kumar, Runjun D. ; Meng, Linyan ; Liu, Pengfei...
American Journal of Medical Genetics Part A.  188 (2022)  11 - p. 3184-3190 , 2022
 
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7

A deep intronic variant is a common cause of OTC deficiency..:

Kumar, Runjun D. ; Burrage, Lindsay C. ; Bartos, Jan...
Molecular Genetics and Metabolism Reports.  26 (2021)  - p. 100706 , 2021
 
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8

A case of p53 related intellectual disability, seizures, mi..:

Kumar, Runjun ; Bertuch, Alison
Molecular Genetics and Metabolism.  132 (2021)  - p. S89-S90 , 2021
 
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11

A TMPRSS2‐ERG gene signature predicts prognosis of patients..:

Zhou, Emily ; Zhang, Baoyi ; Zhu, Kenneth...
Clinical and Translational Medicine.  10 (2020)  8 - p. , 2020
 
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