Vanstone, Megan R
114  Ergebnisse:
Personensuche X
?
3

Neuropathologic Features of Pontocerebellar Hypoplasia Type..:

Joseph, Jeffrey T. ; Innes, A. Micheil ; Smith, Amanda C....
Journal of Neuropathology & Experimental Neurology.  73 (2014)  11 - p. 1009-1025 , 2014
 
?
4

Mutations in PIK3R1 Cause SHORT Syndrome:

Dyment, David A. ; Smith, Amanda C. ; Alcantara, Diana...
The American Journal of Human Genetics.  93 (2013)  1 - p. 158-166 , 2013
 
?
5

International Cooperation to Enable the Diagnosis of All Ra..:

Boycott, Kym M ; Rath, Ana ; Chong, Jessica X...
Boycott , K M , Rath , A , Chong , J X , Hartley , T , Alkuraya , F S , Baynam , G , Brookes , A J , Brudno , M , Carracedo , A , den Dunnen , J T , Dyke , S O M , Estivill , X , Goldblatt , J , Gonthier , C , Groft , S C , Gut , I , Hamosh , A , Hieter , P , Hoehn , S , Hurles , M E , Kaufmann , P , Knoppers , B M , Krischer , J P , Macek , M , Matthijs , G , Olry , A , Parker , S , Paschall , J , Philippakis , A A , Rehm , H L , Robinson , P N , Sham , P-C , Stefanov , R , Taruscio , D , Unni , D , Vanstone , M R , Zhang , F , Brunner , H , Bamshad , M J & Lochmueller , H 2017 , ' International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases ' , American Journal of Human Genetics , vol. 100 , no. 5 , pp. 695-705 . https://doi.org/10.1016/j.ajhg.2017.04.003.  , 2017
 
?
8

Mutations in PIK3R1 Cause SHORT Syndrome:

Dyment, David A ; Smith, Amanda C ; Alcantara, Diana...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3710754.  , 2013
 
?
11

Development of a Patient-Oriented Intervention to Support P..:

Madani Larijani, Maryam ; Dumba, Cindy ; Thiessen, Heather...
International Journal of Environmental Research and Public Health.  18 (2021)  5 - p. 2786 , 2021
 
1-15