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Mallet-Motak, Delphine
18  Ergebnisse:
Personensuche X
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1

News about the genetics of congenital primary adrenal insuf..:

Roucher-Boulez, Florence ; Mallet-Motak, Delphine ; Tardy-Guidollet, Véronique...
Annales d'Endocrinologie.  79 (2018)  3 - p. 174-181 , 2018
Link: https://doi.org/10.1016/..
 
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2

A splicing mutation in the DMD gene detected by next-genera..:

Roucher Boulez, Florence ; Menassa, Rita ; Streichenberger, Nathalie...
Clinica Chimica Acta.  448 (2015)  - p. 146-149 , 2015
Link: https://doi.org/10.1016/..
 
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3

Hypopituitarism in Patients with Blepharophimosis and FOXL2..:

Castets, Sarah ; Roucher-Boulez, Florence ; Saveanu, Alexandru...
info:eu-repo/semantics/altIdentifier/doi/10.1159/000507249.  , 2020
Link: https://hal-amu.archives..
 
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4

Hypopituitarism in Patients with Blepharophimosis and FOXL2..:

Castets, Sarah ; Roucher-Boulez, Florence ; Saveanu, Alexandru...
info:eu-repo/semantics/altIdentifier/doi/10.1159/000507249.  , 2020
Link: https://amu.hal.science/..
 
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5

Hypopituitarism in Patients with Blepharophimosis and FOXL2..:

Castets, Sarah ; Roucher-Boulez, Florence ; Saveanu, Alexandru...
info:eu-repo/semantics/altIdentifier/doi/10.1159/000507249.  , 2020
Link: https://amu.hal.science/..
 
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6

Hypopituitarism in Patients with Blepharophimosis and FOXL2..:

Castets, Sarah ; Roucher-Boulez, Florence ; Saveanu, Alexandru...
info:eu-repo/semantics/altIdentifier/doi/10.1159/000507249.  , 2020
Link: https://amu.hal.science/..
 
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7

Hypopituitarism in Patients with Blepharophimosis and FOXL2..:

Castets, Sarah ; Roucher-Boulez, Florence ; Saveanu, Alexandru...
info:eu-repo/semantics/altIdentifier/doi/10.1159/000507249.  , 2020
Link: https://amu.hal.science/..
 
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8

Hypopituitarism in Patients with Blepharophimosis and FOXL2..:

Castets, Sarah ; Roucher-Boulez, Florence ; Saveanu, Alexandru...
info:eu-repo/semantics/altIdentifier/doi/10.1159/000507249.  , 2020
Link: https://amu.hal.science/..
 
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9

Hypopituitarism in Patients with Blepharophimosis and FOXL2..:

Castets, Sarah ; Roucher-Boulez, Florence ; Saveanu, Alexandru...
info:eu-repo/semantics/altIdentifier/doi/10.1159/000507249.  , 2020
Link: https://amu.hal.science/..
 
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10

NNT mutations: a cause of primary adrenal insufficiency, ox..:

Roucher-Boulez, Florence ; Mallet-Moták, Delphine ; Samara-Boustani, Dinane...
info:eu-repo/semantics/altIdentifier/doi/10.1530/EJE-16-0056.  , 2016
Link: https://univ-rennes.hal...
 
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11

NNT mutations: a cause of primary adrenal insufficiency, ox..:

Roucher-Boulez, Florence ; Mallet-Moták, Delphine ; Samara-Boustani, Dinane...
info:eu-repo/semantics/altIdentifier/doi/10.1530/EJE-16-0056.  , 2016
Link: https://univ-rennes.hal...
 
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12

NNT mutations: a cause of primary adrenal insufficiency, ox..:

Roucher-Boulez, Florence ; Mallet-Moták, Delphine ; Samara-Boustani, Dinane...
info:eu-repo/semantics/altIdentifier/doi/10.1530/EJE-16-0056.  , 2016
Link: https://univ-rennes.hal...
 
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13

NNT mutations: a cause of primary adrenal insufficiency, ox..:

Roucher-Boulez, Florence ; Mallet-Moták, Delphine ; Samara-Boustani, Dinane...
info:eu-repo/semantics/altIdentifier/pmid/27129361.  , 2016
Link: https://hal-univ-rennes1..
 
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14

NNT mutations: a cause of primary adrenal insufficiency, ox..:

Roucher-Boulez, Florence ; Mallet-Moták, Delphine ; Samara-Boustani, Dinane...
info:eu-repo/semantics/altIdentifier/doi/10.1530/EJE-16-0056.  , 2016
Link: https://univ-rennes.hal...
 
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15

NNT mutations: a cause of primary adrenal insufficiency, ox..:

Roucher-Boulez, Florence ; Mallet-Moták, Delphine ; Samara-Boustani, Dinane...
info:eu-repo/semantics/altIdentifier/doi/10.1530/EJE-16-0056.  , 2016
Link: https://hal-univ-rennes1..
 
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