E-LIB Suche - Ergebnisse für: Donovan, Frank

1

Genomic landscape of patients with germline RUNX1 variants ..:

Yu, Kai ; Deuitch, Natalie ; Merguerian, Matthew...
Blood Advances. 8 (2024) 2 - p. 497-511 , 2024

2

Exploration of the role of whole exome sequencing variants ..:

Woo, Elizabeth Geena ; Donovan, Frank ; Stubblefield, Barbara...
Molecular Genetics and Metabolism. 132 (2021) 2 - p. S113 , 2021

Link: https://doi.org/10.1016/..

3

How do we explain very discordant phenotypes among three si..:

Eghbali, Areian ; Garcia, Eric ; Tanima, Yuichiro...
Molecular Genetics and Metabolism. 126 (2019) 2 - p. S51-S52 , 2019

Link: https://doi.org/10.1016/..

4

Methylomic and whole transcriptome analyses reveal several ..:

Garcia, Eric Joshua ; Donovan, Frank ; Elkahloun, Abdel...
Molecular Genetics and Metabolism. 126 (2019) 2 - p. S57 , 2019

Link: https://doi.org/10.1016/..

5

Looking beyond the realm of traditional genetics: DNA methy..:

Hassan, Shahzeb ; Grey, Richard ; Donovan, Frank...
Molecular Genetics and Metabolism. 120 (2017) 1-2 - p. S63 , 2017

Link: https://doi.org/10.1016/..

6

Zauberglaube und Hexenkult

ein historischer Abriss Goldmann Sachbücher. 11124

Donovan, Frank , 1971

Copies: Zentrale:E02 a soz 690/164

7

AP2A2 mutation and defective endocytosis in a Malian family..:

Diarra, Salimata ; Ghosh, Saikat ; Cissé, Lassana...
Neurobiology of Disease. 198 (2024) - p. 106537 , 2024

Link: https://doi.org/10.1016/..

8

FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice var..:

Ramanagoudr-Bhojappa, Ramanagouda ; Tryon, Rebecca ; Lach, Francis P....
Blood Advances. 8 (2024) 4 - p. 899-908 , 2024

Link: https://doi.org/10.1182/..

9

Haplotype-based analysis resolves missing heritability in o..:

Loftus, Stacie K. ; Gillis, Meredith F. ; Lundh, Linnea...
The American Journal of Human Genetics. 110 (2023) 7 - p. 1123-1137 , 2023

Link: https://doi.org/10.1016/..

10

Genomic signature of Fanconi anaemia DNA repair pathway def..:

Webster, Andrew L. H. ; Sanders, Mathijs A. ; Patel, Krupa...
Nature. 612 (2022) 7940 - p. 495-502 , 2022

Link: https://doi.org/10.1038/..

11

The causes of Fanconi anemia in South Asia and the Middle E..:

Thompson, Ashley S. ; Saba, Nusrat ; McReynolds, Lisa J....
Molecular Genetics & Genomic Medicine. 9 (2021) 7 - p. , 2021

Link: https://doi.org/10.1002/..

12

A founder variant in the South Asian population leads to a ..:

Donovan, Frank X. ; Solanki, Avani ; Mori, Minako...
Human Mutation. 41 (2019) 1 - p. 122-128 , 2019

Link: https://doi.org/10.1002/..

13

iPSCs and fibroblast subclones from the same fibroblast pop..:

Kwon, Erika M. ; Connelly, John P. ; Hansen, Nancy F....
Proceedings of the National Academy of Sciences. 114 (2017) 8 - p. 1964-1969 , 2017

Link: https://doi.org/10.1073/..

14

Whole-Exome Sequencing for Diagnosis of Turner Syndrome: To..:

Murdock, David R. ; Donovan, Frank X. ; Chandrasekharappa, Settara C....
The Journal of Clinical Endocrinology & Metabolism. 102 (2017) 5 - p. 1529-1537 , 2017

Link: https://doi.org/10.1210/..

15

iPSCs and fibroblast subclones from the same fibroblast pop..:

Kwon, Erika M. ; Connelly, John P. ; Hansen, Nancy F....
Proceedings of the National Academy of Sciences of the United States of America. 114 (2017) 8 - p. 1964-1969 , 2017

Link: https://www.jstor.org/st..