All individuals with variants in gene PTS

15 entries on 1 page. Showing entries 1 - 15.
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AscendingIndividual ID     

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Gender     

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Age at death     

VIP     

Data_av     

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Disease     

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Variants     

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Owner     
00396458 15013721 PubMed: Ellingford 2017 - - - United Kingdom (Great Britain) - - - - - ? - 1 1 Johan den Dunnen
00402000 MD130 PubMed: Meili 2009 2-generation family, 1 affected, unaffected parents M - Switzerland - - - - - HPA yperphenylalaninaemia, monoamine neurotransmitter deficiency 2 1 Johan den Dunnen
00402001 MD96 PubMed: Meili 2009 2-generation family, 1 affected, unaffected parents F yes Morocco - - - - - HPA found by neonatal screening 1 1 Johan den Dunnen
00421514 A2-O PubMed: Trujillano 2014 - - - Spain - - - - - HPA - 2 1 Johan den Dunnen
00421516 B2-O PubMed: Trujillano 2014 - - - Spain - - - - - HPA - 2 1 Johan den Dunnen
00421518 C2-O PubMed: Trujillano 2014 - - - Spain - - - - - HPA - 1 1 Johan den Dunnen
00421522 H1-O PubMed: Trujillano 2014 - - - Spain - - - - - HPA - 2 1 Johan den Dunnen
00452228 - PubMed: Wang 2019 screening 401,660 newborns for inborn errors of metabolism - - China - - - - - ? - 1 5 Johan den Dunnen
00452229 - PubMed: Wang 2019 screening 401,660 newborns for inborn errors of metabolism - - China - - - - - ? - 1 3 Johan den Dunnen
00452230 - PubMed: Wang 2019 screening 401,660 newborns for inborn errors of metabolism - - China - - - - - ? - 1 1 Johan den Dunnen
00452231 - PubMed: Wang 2019 screening 401,660 newborns for inborn errors of metabolism - - China - - - - - ? - 1 1 Johan den Dunnen
00452232 - PubMed: Wang 2019 screening 401,660 newborns for inborn errors of metabolism - - China - - - - - ? - 1 1 Johan den Dunnen
00452233 - PubMed: Wang 2019 screening 401,660 newborns for inborn errors of metabolism - - China - - - - - ? - 1 1 Johan den Dunnen
00453714 Pat141 PubMed: Navarrete 2019 newborn screening - - Spain - - - - - metabolic syndrome see paper; ..., newborn screening tandem mass spectrometry dried blood spots 2 1 Johan den Dunnen
00466214 Pat4 PubMed: Soriano-Sexto 2022, Journal: Soriano-Sexto 2022 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Spain - - - - - ? see paper; ..., hyperphenylalaninemia 3 1 Johan den Dunnen
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