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Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles[BRAF-positive paucicellular variant of anaplastic carcinoma in the presence of tall cell variant papillary thyroid cancer].[Ataxia with oculomotor apraxia type 4 detected by next-generation sequencing].Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders.Molecular markers based on LTR retrotransposons BARE-1 and Jeli uncover different strata of evolutionary relationships in diploid wheatsDe novo nonsense mutation in WHSC1 (NSD2) in patient with intellectual disability and dysmorphic features[New allelic variants of non-syndromic mental retardation of type 20 caused by mutations in the MEF2C gene]
P50
Q28117017-5BA1ADFC-98D1-493A-A05C-82F3179294D3Q40153152-D68ED643-22D3-45C7-923C-0C1E7461D4ABQ52590197-EB9EA236-5CC4-43EB-A202-0B7938A12020Q52674255-B0EFEA32-644F-4685-B4B4-4342557F024EQ84083668-0899467F-43BB-4596-88F4-132D1844A881Q88671339-E18346A1-90B7-4056-BACC-1417C5627E2AQ88972636-F69C078D-A458-4958-977F-BDA64FEF9199
P50
description
researcher ORCID ID = 0000-0001-6414-436X
@en
name
Fedor A Konovalov
@ast
Fedor A Konovalov
@en
Fedor A Konovalov
@es
Fedor A Konovalov
@nl
type
label
Fedor A Konovalov
@ast
Fedor A Konovalov
@en
Fedor A Konovalov
@es
Fedor A Konovalov
@nl
prefLabel
Fedor A Konovalov
@ast
Fedor A Konovalov
@en
Fedor A Konovalov
@es
Fedor A Konovalov
@nl
P1153
6603311886
P31
P496
0000-0001-6414-436X