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Morel, Godelieve
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1

Prenatal and neonatal phenotype of Larsen of La Réunion Isl..:

Alessandri, Jean-Luc ; Celse, Tristan ; Spodenkiewicz, Marta...
European Journal of Medical Genetics.  69 (2024)  - p. 104940 , 2024
Link: https://doi.org/10.1016/..
 
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2

First Description of a Large Clinical Series of Fetal Alcoh..:

Sennsfelder, Laëtitia ; Guilly, Susie ; Henkous, Sonia...
Children.  11 (2024)  8 - p. 955 , 2024
Link: https://doi.org/10.3390/..
 
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3

Prenatal exome sequencing, a powerful tool for improving th..:

Thauvin‐Robinet, Christel ; Garde, Aurore ; Delanne, Julian...
Prenatal Diagnosis.  , 2024
Link: https://doi.org/10.1002/..
 
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4

Description of Copy Number Variations in a Series of Childr..:

Sennsfelder, Laëtitia ; Guilly, Susie ; Leruste, Sébastien...
Children.  10 (2023)  4 - p. 694 , 2023
Link: https://doi.org/10.3390/..
 
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5

RIPOR2: A new gene of non‐syndromic cochleovestibular dysfu..:

Morel, Godelieve ; Ernest, Sylvain ; Serey‐Gaut, Margaux...
Clinical Genetics.  104 (2023)  6 - p. 669-673 , 2023
Link: https://doi.org/10.1111/..
 
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6

Correction to: Evaluation of somatic and/or germline mosaic..:

Chesneau, Bertrand ; Ivashchenko, Véronique ; Habib, Christophe...
European Journal of Human Genetics.  31 (2022)  5 - p. 607-607 , 2022
Link: https://doi.org/10.1038/..
 
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7

STAC3 related congenital myopathy: A case series of seven C..:

Gromand, Marie ; Gueguen, Paul ; Pervillé, Anne...
European Journal of Medical Genetics.  65 (2022)  10 - p. 104598 , 2022
Link: https://doi.org/10.1016/..
 
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8

Refining the clinical phenotype associated with missense va..:

Tharreau, Mylène ; Garde, Aurore ; Marlin, Sandrine...
American Journal of Medical Genetics Part A.  188 (2022)  5 - p. 1600-1606 , 2022
Link: https://doi.org/10.1002/..
 
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9

First evidence of SOX2 mutations in Peters' anomaly: Lesson..:

Chesneau, Bertrand ; Aubert‐Mucca, Marion ; Fremont, Félix...
Clinical Genetics.  101 (2022)  5-6 - p. 494-506 , 2022
Link: https://doi.org/10.1111/..
 
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10

Evaluation of somatic and/or germline mosaicism in congenit..:

Chesneau, Bertrand ; Ivashchenko, Véronique ; Habib, Christophe...
European Journal of Human Genetics.  31 (2022)  5 - p. 526-530 , 2022
Link: https://doi.org/10.1038/..
 
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11

Growth charts in Cockayne syndrome type 1 and type 2:

Baer, Sarah ; Tuzin, Nicolas ; Kang, Peter B....
European Journal of Medical Genetics.  64 (2021)  1 - p. 104105 , 2021
Link: https://doi.org/10.1016/..
 
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12

Outcomes of 4 years of molecular genetic diagnosis on a pan..:

Grelet, Maude ; Blanck, Véronique ; Sigaudy, Sabine...
Orphanet Journal of Rare Diseases.  14 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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13

A new mutation in the mitochondrial tRNAPro gene associated..:

Morel, Godelieve ; Bannwarth, Sylvie ; Chaussenot, Annabelle...
Neuromuscular Disorders.  26 (2016)  12 - p. 885-889 , 2016
Link: https://doi.org/10.1016/..
 
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14

CHCHD10 mutations are not a common cause of SMN1‐negative t..:

Morel, Godelieve ; Rouzier, Cécile ; Chaussenot, Annabelle...
Annals of Neurology.  78 (2015)  5 - p. 831-831 , 2015
Link: https://doi.org/10.1002/..
 
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15

Episignatures in practice: independent evaluation of publis..:

Husson, Thomas ; Lecoquierre, François ; Nicolas, Gaël...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-023-01474-x.  , 2024
Link: https://univ-rennes.hal...
 
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