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David, Dezső
345  Ergebnisse:
Personensuche X
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1

Balanced chromosomal rearrangements implicate YIPF5 and SPA..:

David, Dezső ; Fino, Joana ; Oliveira, Renata..
Gene.  887 (2023)  - p. 147737 , 2023
Link: https://doi.org/10.1016/..
 
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2

Editorial: Chromosome structural variants: Epidemiology, id..:

Dong, Zirui ; David, Dezso ; Gonzaga-Jauregui, Claudia..
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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3

Corrigendum: SVInterpreter: A Comprehensive Topologically A..:

Fino, Joana ; Marques, Bárbara ; Dong, Zirui.
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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4

A Novel Frameshift CHD4 Variant Leading to Sifrim-Hitz-Weis..:

Da Silva, Jorge Diogo ; Oliva-Teles, Natália ; Tkachenko, Nataliya...
Biomedicines.  11 (2022)  1 - p. 12 , 2022
Link: https://doi.org/10.3390/..
 
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5

SVInterpreter: A Comprehensive Topologically Associated Dom..:

Fino, Joana ; Marques, Bárbara ; Dong, Zirui.
Frontiers in Genetics.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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6

Clinical and genetic findings in Hungarian pediatric patien..:

Lengyel, Anna ; Pinti, Éva ; Pikó, Henriett...
European Journal of Medical Genetics.  63 (2020)  10 - p. 104027 , 2020
Link: https://doi.org/10.1016/..
 
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7

Comprehensive clinically oriented workflow for nucleotide l..:

David, Dezső ; Freixo, João P. ; Fino, Joana...
Human Genetics.  139 (2020)  4 - p. 531-543 , 2020
Link: https://doi.org/10.1007/..
 
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8

Ring chromosome 6 in a child with anterior segment dysgenes..:

Corona‐Rivera, Jorge Román ; Corona‐Rivera, Alfredo ; Zepeda‐Romero, Luz Consuelo...
Congenital Anomalies.  59 (2018)  5 - p. 174-178 , 2018
Link: https://doi.org/10.1111/..
 
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9

Identification of OAF and PVRL1 as candidate genes for an o..:

David, Dezső ; Anand, Deepti ; Araújo, Carlos...
Experimental Eye Research.  168 (2018)  - p. 161-170 , 2018
Link: https://doi.org/10.1016/..
 
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10

Complex X chromosome rearrangement associated with multiorg..:

Haltrich, Irén ; Pikó, Henriett ; Pamjav, Horolma...
Molecular Cytogenetics.  8 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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11

Co-segregation of trichorhinophalangeal syndrome with a t(8..:

David, Dezső ; Marques, Bárbara ; Ferreira, Cristina...
Human Genetics.  132 (2013)  11 - p. 1287-1299 , 2013
Link: https://doi.org/10.1007/..
 
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12

Genetic defects in Portuguese families with inherited prote..:

David, Dezső ; Ferreira, Cristina ; Ventura, Célia...
Thrombosis Research.  128 (2011)  3 - p. 299-302 , 2011
Link: https://doi.org/10.1016/..
 
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13

Molecular basis of inherited antithrombin deficiency in Por..:

David, Dezsö ; Ribeiro, Sofia ; Ferrão, Lénia..
American Journal of Hematology.  76 (2004)  2 - p. 163-171 , 2004
Link: https://doi.org/10.1002/..
 
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14

Molecular characterization of a familial translocation impl..:

David, Dezsö ; Cardoso, Joana ; Marques, B.árbara...
Genomics.  81 (2003)  5 - p. 489-503 , 2003
Link: https://doi.org/10.1016/..
 
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15

Molecular characterization of a 7p15–21 homozygous deletion..:

Sossey‐Alaoui, Khalid ; Vieira, Luís ; David, Dezso..
Genes, Chromosomes and Cancer.  36 (2002)  1 - p. 1-6 , 2002
Link: https://doi.org/10.1002/..
 
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