Baris, Hagit N.
196  results:
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2

Identification of a novel PCNT founder pathogenic variant i..:

Weiss, Karin ; Ekhilevitch, Nina ; Cohen, Lior...
European Journal of Medical Genetics.  63 (2020)  2 - p. 103643 , 2020
 
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7

Mutations in the mitochondrial ribosomal protein MRPS22 lea..:

Chen, Anlu ; Tiosano, Dov ; Guran, Tulay...
Human Molecular Genetics.  27 (2018)  11 - p. 1913-1926 , 2018
 
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9

Rare Disease Diagnostics: A Single-center Experience and Le..:

Weiss, Karin ; Kurolap, Alina ; Paperna, Tamar...
Rambam Maimonides Medical Journal.  9 (2018)  3 - p. e0018 , 2018
 
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10

Trio approach reveals higher risk of PD in carriers of seve..:

Arkadir, David ; Dinur, Tama ; Mullin, Stephen...
Blood Cells, Molecules, and Diseases.  68 (2018)  - p. 115-116 , 2018
 
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15

Is one diagnosis the whole story? patients with double diag..:

Kurolap, Alina ; Orenstein, Naama ; Kedar, Inbal...
American Journal of Medical Genetics Part A.  170 (2016)  9 - p. 2338-2348 , 2016
 
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