Hurles, Matthew
335  Ergebnisse:
Personensuche X
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2

Prevalence of deleterious variants in MC3R in patients with..:

Duckett, Katie ; Williamson, Alice ; Kincaid, John...
Duckett , K , Williamson , A , Kincaid , J , Rainbow , K , Lam , B , Corbin , L J , Martin , H C , Eberhardt , R Y , Huang , Q Q , Hurles , M , Brauner , R , Delaney , A , McElreavey , K , Hall , J , Hirschhorn , J N , Palmert , M , Seminara , S , Banerjee , I , Perry , J R B , Timpson , N J , Clayton , P , Chan , Y-M , Ong , K K & O'Rahilly , S 2023 , ' Prevalence of deleterious variants in MC3R in patients with constitutional delay of growth and puberty ' , Journal of Clinical Endocrinology and Metabolism , vol. 108 , no. 12 , dgad373 , pp. e1580-e1587 . https://doi.org/10.1210/clinem/dgad373.  , 2023
 
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8

Genetic correlates of phenotypic heterogeneity in autism:

Warrier, Varun ; Zhang, Xinhe ; Reed, Patrick...
info:eu-repo/semantics/altIdentifier/doi/10.1101/2020.07.21.20159228.  , 2021
 
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9

Loss of ADAMTS19 causes progressive non-syndromic heart val..:

Wünnemann, Florian ; Ta-Shma, Asaf ; Preuss, Christoph...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41588-019-0536-2.  , 2020
 
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10

Loss of ADAMTS19 causes progressive non-syndromic heart val..:

Wünnemann, Florian ; Ta-Shma, Asaf ; Preuss, Christoph...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41588-019-0536-2.  , 2020
 
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13

Registered access: authorizing data access:

Dyke, Stephanie O.M ; Linden, Mikael ; Lappalainen, Ilkka...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-018-0219-y.  , 2018
 
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14

Registered access: authorizing data access:

Dyke, Stephanie O. M ; Linden, Mikael ; Lappalainen, Ilkka...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244209/.  , 2018
 
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