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Xenia Latypova
120  results:
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1

Biallelic USP14 variants cause a syndromic neurodevelopment..:

Ebstein, Frédéric ; Latypova, Xenia ; Sharon Hung, Ka Ying...
Genetics in Medicine.  26 (2024)  6 - p. 101120 , 2024
Link: https://doi.org/10.1016/..
 
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2

Challenges of preconception genetic testing in France: A qu..:

Hoarau, Eugénie ; Latypova, Xenia ; Jourdain, Maud.
European Journal of Medical Genetics.  65 (2022)  11 - p. 104606 , 2022
Link: https://doi.org/10.1016/..
 
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3

NGS-driven molecular diagnosis of heterogeneous hereditary ..:

Khan, Ayaz ; Tian, Shixiong ; Tariq, Muhammad...
Molecular Genetics and Genomics.  297 (2022)  6 - p. 1601-1613 , 2022
Link: https://doi.org/10.1007/..
 
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4

Pathogenic variants in SLF2 and SMC5 cause segmented chromo..:

Grange, Laura J. ; Reynolds, John J. ; Ullah, Farid...
Nature Communications.  13 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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5

Objective Evaluation of Clinical Actionability for Genes In..:

Vecten, Maude ; Pion, Emmanuelle ; Bartoli, Marc...
International Journal of Molecular Sciences.  23 (2022)  15 - p. 8506 , 2022
Link: https://doi.org/10.3390/..
 
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6

Letter regarding the article "two girls with short stature,..:

Latypova, Xenia ; Dang, Xiao ; Zhang, Jianguo.
European Journal of Medical Genetics.  64 (2021)  4 - p. 104179 , 2021
Link: https://doi.org/10.1016/..
 
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7

A Genomic Approach to Delineating the Occurrence of Scolios..:

Latypova, Xenia ; Creadore, Stefan Giovanni ; Dahan-Oliel, Noémi...
Genes.  12 (2021)  7 - p. 1052 , 2021
Link: https://doi.org/10.3390/..
 
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8

First French study relative to preconception genetic testin..:

Bonneau, Valérie ; Nizon, Mathilde ; Latypova, Xenia...
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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9

The Clinical and Genotypic Spectrum of Scoliosis in Multipl..:

Dahan-Oliel, Noémi ; Dieterich, Klaus ; Rauch, Frank...
Genes.  12 (2021)  8 - p. 1220 , 2021
Link: https://doi.org/10.3390/..
 
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10

A dominant vimentin variant causes a rare syndrome with pre..:

Cogné, Benjamin ; Bouameur, Jamal-Eddine ; Hayot, Gaëlle...
European Journal of Human Genetics.  28 (2020)  9 - p. 1218-1230 , 2020
Link: https://doi.org/10.1038/..
 
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11

Familial deep endometriosis: A rare monogenic disease?:

Isidor, Bertrand ; Latypova, Xenia ; Ploteau, Stéphane
European Journal of Obstetrics & Gynecology and Reproductive Biology.  221 (2018)  - p. 190-193 , 2018
Link: https://doi.org/10.1016/..
 
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12

New splicing pathogenic variant in EBP causing extreme fami..:

Pacault, Mathilde ; Vincent, Marie ; Besnard, Thomas...
European Journal of Human Genetics.  26 (2018)  12 - p. 1784-1790 , 2018
Link: https://doi.org/10.1038/..
 
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13

Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 gove..:

Szenker-Ravi, Emmanuelle ; Altunoglu, Umut ; Leushacke, Marc...
Nature.  561 (2018)  7722 - p. E7-E7 , 2018
Link: https://doi.org/10.1038/..
 
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14

RSPO2 inhibition of RNF43 and ZNRF3 governs limb developmen..:

Szenker-Ravi, Emmanuelle ; Altunoglu, Umut ; Leushacke, Marc...
Nature.  557 (2018)  7706 - p. 564-569 , 2018
Link: https://doi.org/10.1038/..
 
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15

Correction: Corrigendum: Novel KCNB1 mutation associated wi..:

Latypova, Xénia ; Matsumoto, Naomichi ; Vinceslas-Muller, Cécile...
Journal of Human Genetics.  62 (2017)  5 - p. 585-585 , 2017
Link: https://doi.org/10.1038/..
 
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