Cenni, Camille
10  results:
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1

Association of Meier-Gorlin and microcephalic osteodysplast..:

Sabbagh, Quentin ; Tharreau, Mylène ; Cenni, Camille...
European Journal of Medical Genetics.  66 (2023)  5 - p. 104733 , 2023
 
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2

TBX3 and TBX5 duplication: A family with an atypical overla..:

Cenni, Camille ; Andres, Stephanie ; Hempel, Maja...
European Journal of Medical Genetics.  64 (2021)  7 - p. 104213 , 2021
 
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4

When Familial Hearing Loss Means Genetic Heterogeneity: A M..:

Cenni, Camille ; Mansard, Luke ; Blanchet, Catherine...
info:eu-repo/semantics/altIdentifier/doi/10.3390/diagnostics11091636.  , 2021
 
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5

When Familial Hearing Loss Means Genetic Heterogeneity: A M..:

Cenni, Camille ; Mansard, Luke ; Blanchet, Catherine...
info:eu-repo/semantics/altIdentifier/doi/10.3390/diagnostics11091636.  , 2021
 
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6

When Familial Hearing Loss Means Genetic Heterogeneity: A M..:

Cenni, Camille ; Mansard, Luke ; Blanchet, Catherine...
info:eu-repo/semantics/altIdentifier/doi/10.3390/diagnostics11091636.  , 2021
 
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7

When Familial Hearing Loss Means Genetic Heterogeneity: A M..:

Cenni, Camille ; Mansard, Luke ; Blanchet, Catherine...
info:eu-repo/semantics/altIdentifier/doi/10.3390/diagnostics11091636.  , 2021
 
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