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Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth.
Not available
S-EPMC4527483
|
biostudies-literature
Cite
Transcatheter Aortic Valve Implantation by Valve Type in Women With Small Annuli: Results From the SMART Randomized Clinical Trial.
Not available
S-EPMC11581526
|
biostudies-literature
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A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome.
Not available
S-EPMC10081357
|
biostudies-literature
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A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome.
Not available
S-EPMC10415337
|
biostudies-literature
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Auto-deconvolution and molecular networking of gas chromatography-mass spectrometry data.
Not available
S-EPMC7971188
|
biostudies-literature
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The LRRK2 p.L1795F variant causes Parkinson's disease in the European population.
Not available
S-EPMC11937388
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biostudies-literature
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Natural History of Vanishing White Matter.
Not available
S-EPMC6175238
|
biostudies-literature
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Expert range maps of global mammal distributions harmonised to three taxonomic authorities.
Not available
S-EPMC9060555
|
biostudies-literature
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Incisional hernia following colorectal cancer surgery according to suture technique: Hughes Abdominal Repair Randomized Trial (HART).
Not available
S-EPMC10364691
|
biostudies-literature
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A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study.
Not available
S-EPMC8576477
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biostudies-literature
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