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2021
[x]
Sacherschließung
Genetics research
(13)
Humans [MeSH]
(10)
Article
(6)
Male [MeSH]
(3)
Child, Preschool [MeSH]
(3)
Child [MeSH]
(3)
Letter
(2)
Genetic testing
(2)
Genetic Predisposition to Disease [MeSH]
(2)
Female [MeSH]
(2)
Publikationstyp
Artikel
(13)
Medium
Erscheinungsjahr
Institution
13 Treffer
Seiten
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Kurzansicht
E-Jahr
Zugriff
Typ
Operations
Effect of a common UMOD variant on kidney function, blood pressure, cognitive and physical function in a community-based cohort of older adults
2021 .
villagomez fuentes, linda elizabeth
|
Algharably, Engi Abdel–Hady
|
Toepfer, Sarah
|
König, Maximilian
|
Demuth, Ilja
|
Bertram, Lars
|
Kreutz, Reinhold
|
Bolbrinker, Juliane
2021
http://purl.org/ontology/bibo/Article
Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3—a subgroup of K+ channelopathies
2021 .
Gripp, Karen
|
Smithson, Sarah F.
|
Scurr, Ingrid J.
|
Baptista, Julia
|
Majumdar, Anirban
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Pierre, Germaine
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Williams, Maggie
|
Henderson, Lindsay B.
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Wentzensen, Ingrid M.
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McLaughlin, Heather
|
Leeuwen, Lisette
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Simon, Marleen E. H.
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van Binsbergen, Ellen
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Dinulos, Mary Beth P.
|
Kaplan, Julie D.
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McRae, Anne
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Superti-Furga, Andrea
|
Good, Jean-Marc
|
, Kerstin
2021
http://purl.org/ontology/bibo/Article
Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li–Fraumeni syndrome
2021 .
Winter, Greta
|
Kirschner-Schwabe, Renate
|
Groeneveld-Krentz, Stefanie
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Escherich, Gabriele
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Möricke, Anja
|
von Stackelberg, Arend
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Stanulla, Martin
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Bailey, Simon
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Richter, Lisa
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Steinemann, Doris
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Ripperger, Tim
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Escudero, Adela
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Farah, Roula
|
Lohi, Olli
|
Wadt, Karin
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Jongmans, Marjolijn
|
van Engelen, Nienke
|
Eckert, Cornelia
|
Kratz, Christian
2021
http://purl.org/ontology/bibo/Article
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
2021 .
Decker, Melanie
|
Lammens, Tim
|
Ferster, Alina
|
Erlacher, Miriam
|
Yoshimi, Ayami
|
Niemeyer, Charlotte
|
Ernst, Martijn P. T.
|
Raaijmakers, Marc H. G. P.
|
Duployez, Nicolas
|
Flaum, Andreas
|
Steinemann, Doris
|
Schlegelberger, Brigitte
|
Illig, Thomas
|
Ripperger, Tim
2021
http://purl.org/ontology/bibo/Article
Novel bi-allelic variants expand the SPTBN4-related genetic and phenotypic spectrum
2021 .
Buelow, Markus
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Süßmuth, David
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Smith, Laurie D.
|
Aryani, Omid
|
CASTIGLIONI, CLAUDIA
|
Stenzel, Werner
|
Bertini, Enrico
|
Schuelke, Markus
|
Knierim, Ellen
2021
http://purl.org/ontology/bibo/Article
Exome first approach to reduce diagnostic costs and time – retrospective analysis of 111 individuals with rare neurodevelopmental disorders
2021 .
Klau, Julia
|
Abou Jamra, Rami
|
Radtke, Maximilian
|
Oppermann, Henry
|
Lemke, Johannes
|
Beblo, Skadi
|
Popp, Bernt
2021
http://purl.org/ontology/bibo/Article
Familial cleft tongue caused by a unique translation initiation codon variant in TP63
2021 .
Schmidt, Julia
|
Schreiber, Gudrun
|
Altmüller, Janine
|
Thiele, Holger
|
Nürnberg, Peter
|
Li, Yun
|
Kaulfuß, Silke
|
Funke, Rudolf
|
Wilken, Bernd
|
Yigit, Gökhan
|
Wollnik, Bernd
2021
http://purl.org/ontology/bibo/Article
The acrocentric part of der(Y)t(Y;acro)(q12;p1?2) contains D15Z1 sequences in the majority of cases
2021 .
Fuchs, Sigrid
|
Lisfeld, Jasmin
|
Kankel, Stefanie
|
Person, Luisa
|
Liehr, Thomas
2021
http://purl.org/ontology/bibo/Article
Context-specific chromatin remodeling activity of mSWI/SNF complexes depends on the epigenetic landscape
2021 .
Sokpor, Godwin
|
Nguyen, Huu Phuc
|
Tuoc, Tran
2021
http://purl.org/ontology/bibo/Article
Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain
2021 .
Neuser, Sonja
|
krey, ilona
|
Schwan, Annemarie
|
Abou Jamra, Rami
|
Bartolomaeus, Tobias
|
Döring, Jan
|
Syrbe, Steffen
|
Plassmann, Margit
|
Rohde, Stefan
|
Roth, Christian
|
Rehder, Helga
|
Radtke, Maximilian
|
Le Duc, Diana
|
Schubert, Susanna
|
Bermudez-Guzman, Luis
|
Leal, Alejandro
|
Schoner, Katharina
|
Popp, Bernt
2021
http://purl.org/ontology/bibo/Article
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