Alon, Nitay
10  Ergebnisse:
Personensuche X
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3

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Sever..:

Thompson, Kyle ; Majd, Homa ; Dallabona, Cristina...
The American Journal of Human Genetics.  99 (2016)  6 - p. 1405 , 2016
 
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4

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Sever..:

Thompson, Kyle ; Majd, Homa ; Dallabona, Cristina...
The American Journal of Human Genetics.  99 (2016)  4 - p. 860-876 , 2016
 
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5

The efficacy of a test and ESS program:

Katz, Asaf ; Argov, Nitay ; Shapira, Alon..
Quality and Reliability Engineering International.  18 (2002)  2 - p. 99-109 , 2002
 
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7

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Sever..:

Thompson, Kyle ; Majd, Homa ; Dallabona, Christina...
Thompson , K , Majd , H , Dallabona , C , Reinson , K , King , MS , Alston , CL , He , L , Lodi , T , Jones , SA , Fattal-Valevski , A , Fraenkel , ND , Saada , A , Haham , A , Isohanni , P , Vara , R , Barbosa , IA , Simpson , M A , Deshpande , C , Puusepp , S , Bonnen , PE , Rodenburg , RJ , Suomalainen , A , Õunap , K , Elpeleg , O , Ferrero , I , McFarland , R , Kunji , ER S & Taylor , RW 2016 , ' Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number ' , American Journal of Human Genetics , vol. 99 , no. 4 , pp. 860–876 . https://doi.org/10.1016/j.ajhg.2016.08.014.  , 2016
 
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10

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Sever..:

Thompson, Kyle ; Majd, Homa ; Dallabona, Christina...
Thompson , K , Majd , H , Dallabona , C , Reinson , K , King , MS , Alston , CL , He , L , Lodi , T , Jones , SA , Fattal-Valevski , A , Fraenkel , ND , Saada , A , Haham , A , Isohanni , P , Vara , R , Barbosa , IA , Simpson , M A , Deshpande , C , Puusepp , S , Bonnen , PE , Rodenburg , RJ , Suomalainen , A , Õunap , K , Elpeleg , O , Ferrero , I , McFarland , R , Kunji , ER S & Taylor , RW 2016 , ' Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number ' , American Journal of Human Genetics , vol. 99 , no. 4 , pp. 860–876 . https://doi.org/10.1016/j.ajhg.2016.08.014.  , 2016
 
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