I agree that this site is using cookies. You can find further informations here.
X
Caberg, Jean-Hubert
97  results:
Search for persons X
?
1

Assortative mating and parental genetic relatedness contrib..:

Smolen, Corrine ; Jensen, Matthew ; Dyer, Lisa...
The American Journal of Human Genetics.  110 (2023)  12 - p. 2015-2028 , 2023
Link: https://doi.org/10.1016/..
 
?
2

Newborn screening of SMA: Why and how?:

Dangouloff, Tamara ; Boemer, François ; Caberg, Jean-Hubert..
Journal of the Neurological Sciences.  455 (2023)  - p. 121005 , 2023
Link: https://doi.org/10.1016/..
 
?
3

Novel Loss of Function Variant in BCKDK Causes a Treatable ..:

Boemer, François ; Josse, Claire ; Luis, Géraldine...
International Journal of Molecular Sciences.  23 (2022)  4 - p. 2253 , 2022
Link: https://doi.org/10.3390/..
 
?
4

Three years pilot of spinal muscular atrophy newborn screen..:

Boemer, François ; Caberg, Jean-Hubert ; Beckers, Pablo...
Scientific Reports.  11 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
?
5

The relevance of deep genomic analyses in families with var..:

Pizzo, Lucilla ; Jensen, Matthew ; Tyryshkina, Anastasia...
Molecular Genetics and Metabolism.  132 (2021)  - p. S69 , 2021
Link: https://doi.org/10.1016/..
 
?
6

Newborn screening of duchenne muscular dystrophy specifical..:

Beckers, Pablo ; Caberg, Jean-Hubert ; Dideberg, Vinciane...
Scientific Reports.  11 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
?
7

Correspondence on: "Discrepancy in Spinal Muscular Atrophy ..:

Dangouloff, Tamara ; Boemer, François ; Caberg, Jean-Hubert.
Genetics in Medicine.  22 (2020)  11 - p. 1913-1914 , 2020
Link: https://doi.org/10.1038/..
 
?
8

Reader response: Discrepancy in redetermination ofSMN2copy ..:

Dangouloff, Tamara ; Boemer, François ; Dideberg, Vinciane..
Neurology.  95 (2020)  3 - p. 144-145 , 2020
Link: https://doi.org/10.1212/..
 
?
9

Newborn screening for SMA in Southern Belgium:

Boemer, François ; Caberg, Jean-Hubert ; Dideberg, Vinciane...
Neuromuscular Disorders.  29 (2019)  5 - p. 343-349 , 2019
Link: https://doi.org/10.1016/..
 
?
10

VPS51 biallelic variants cause microcephaly with brain malf..:

Uwineza, Annette ; Caberg, Jean-Hubert ; Hitayezu, Janvier...
European Journal of Medical Genetics.  62 (2019)  8 - p. 103704 , 2019
Link: https://doi.org/10.1016/..
 
?
11

Developmental trajectories of neuroanatomical alterations a..:

Cárdenas-de-la-Parra, Alonso ; Martin-Brevet, Sandra ; Moreau, Clara...
NeuroImage.  203 (2019)  - p. 116155 , 2019
Link: https://doi.org/10.1016/..
 
?
12

Transcriptome-wide analysis of natural antisense transcript..:

Wenric, Stephane ; ElGuendi, Sonia ; Caberg, Jean-Hubert...
Scientific Reports.  7 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
?
13

Combined treatment with octreotide LAR and pegvisomant in p..:

Mangupli, Ruth ; Rostomyan, Liliya ; Castermans, Emilie...
Pituitary.  19 (2016)  5 - p. 507-514 , 2016
Link: https://doi.org/10.1007/..
 
?
14

Exome copy number variation detection: Use of a pool of unr..:

Wenric, Stephane ; Sticca, Tiberio ; Caberg, Jean-Hubert...
Genetic Epidemiology.  41 (2016)  1 - p. 35-40 , 2016
Link: https://doi.org/10.1002/..
 
?
15

Cytogenetic Studies of Rwandan Pediatric Patients Presentin..:

Uwineza, Annette ; Hitayezu, Janvier ; Jamar, Mauricette...
Journal of Tropical Pediatrics.  62 (2015)  1 - p. 38-45 , 2015
Link: https://doi.org/10.1093/..
 
1-15