E-LIB Suche - Ergebnisse für: Choucair, Nancy

1

Homozygous microdeletion of the ERI1 and MFHAS1 genes in a ..:

Choucair, Nancy ; Rajab, Mariam ; Mégarbané, André.
American Journal of Medical Genetics Part A. 173 (2017) 7 - p. 1955-1960 , 2017

Link: https://doi.org/10.1002/..

2

Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome: o..:

Mégarbané, André ; Al-Ali, Rashid ; Choucair, Nancy...
BMC Medical Genetics. 17 (2016) 1 - p. , 2016

Link: https://doi.org/10.1186/..

3

Evidence that homozygous PTPRD gene microdeletion causes tr..:

Choucair, Nancy ; Mignon-Ravix, Cecile ; Cacciagli, Pierre...
Molecular Cytogenetics. 8 (2015) 1 - p. , 2015

Link: https://doi.org/10.1186/..

4

10q26.1 Microdeletion: Redefining the critical regions for ..:

Choucair, Nancy ; Abou Ghoch, Joelle ; Fawaz, Ali..
American Journal of Medical Genetics Part A. 167 (2015) 11 - p. 2707-2713 , 2015

Link: https://doi.org/10.1002/..

5

Contribution of copy number variants (CNVs) to congenital, ..:

Choucair, Nancy ; Ghoch, Joelle Abou ; Corbani, Sandra...
Molecular Cytogenetics. 8 (2015) 1 - p. , 2015

Link: https://doi.org/10.1186/..

6

Intragenic rearrangements in X‐linked intellectual deficien..:

Mignon‐Ravix, Cécile ; Cacciagli, Pierre ; Choucair, Nancy...
American Journal of Medical Genetics Part A. 164 (2014) 8 - p. 1991-1997 , 2014

Link: https://doi.org/10.1002/..

7

Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome: o..:

Mégarbané, André ; Al-Ali, Rashid ; Choucair, Nancy...
http://www.biomedcentral.com/1471-2350/17/42. , 2016

Link: http://www.biomedcentral..

8

Evidence that homozygous PTPRD gene microdeletion causes tr..:

Choucair, Nancy ; Mignon-Ravix, Cecile ; Cacciagli, Pierre...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13039-015-0149-0. , 2015

Link: https://amu.hal.science/..

9

Contribution of copy number variants (CNVs) to congenital, ..:

Choucair, Nancy ; Ghoch, Joelle ; Corbani, Sandra...
http://www.molecularcytogenetics.org/content/8/1/26. , 2015

Link: http://www.molecularcyto..

10

Contribution of copy number variants (CNVs) to congenital, ..:

Choucair, Nancy ; Abou Ghoch, Joelle ; Corbani, Sandra...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13039-015-0130-y. , 2015

Link: https://hal-amu.archives..

11

Evidence that homozygous PTPRD gene microdeletion causes tr..:

Choucair, Nancy ; Mignon-Ravix, Cecile ; Cacciagli, Pierre...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13039-015-0149-0. , 2015

Link: https://hal-amu.archives..

12

Contribution of copy number variants (CNVs) to congenital, ..:

Choucair, Nancy ; Abou Ghoch, Joelle ; Corbani, Sandra...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13039-015-0130-y. , 2015

Link: https://amu.hal.science/..

13

Evidence that homozygous PTPRD gene microdeletion causes tr..:

Choucair, Nancy ; Mignon-Ravix, Cecile ; Cacciagli, Pierre...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13039-015-0149-0. , 2015

Link: https://hal-amu.archives..

14

Evidence that homozygous PTPRD gene microdeletion causes tr..:

Choucair, Nancy ; Mignon-Ravix, Cecile ; Cacciagli, Pierre...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13039-015-0149-0. , 2015

Link: https://amu.hal.science/..

15

Contribution of copy number variants (CNVs) to congenital, ..:

Choucair, Nancy ; Abou Ghoch, Joelle ; Corbani, Sandra...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13039-015-0130-y. , 2015

Link: https://hal-amu.archives..