Fanny Kortüm und Goldstein - Info zur Person

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Network and Gene Tools Help Quickly Identify New, Rare ...Newswise

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— Kurki, Alexander Hoischen, Anna C. Need, David B. Goldstein, and Fanny Kortüm. The work received support from the UDN (1U01HG ) and ...

Network and Gene Tools Help Quickly Identify New, Rare ...Duke Health

corporate.dukehealth.org

— Goldstein, and Fanny Kortüm. The work received support from the UDN (1U01HG ) and the Deutsche Forschungsgemeinschaft (KO ) ...

De Novo Truncating Variants in ASXL2 Are Associated with ...Cell

www.cell.com

von V Shashi · · Zitiert von: 13 — Goldstein, and Fanny Kortüm. (The American Journal of Human Genetics 99, 991–999; October 6, 2016). In the originally published version of this article, Table ...

The core FOXG1 syndrome phenotype consists of ...Archive ouverte HAL

hal.science

von F Kortüm · · Zitiert von: 252 — Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina. Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger ...

The core FOXG1 syndrome phenotype consists of postnatal …

research.uni-luebeck.de

NettetFanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch ...

De Novo Truncating Variants in ASXL2 Are Associated with a Unique and...

core.ac.uk

... Korpi-Heikkilä, Olli Pietilainen, Palotie Aarno, Mitja I. Kurki, Alexander Hoischen, Anna C. Need, David B. Goldstein, Fanny Kortüm, A. Bacino, Brendan H. Lee, ...

The core FOXG1 syndrome phenotype consists of ...CORE

core.ac.uk

von F Kortüm · · Zitiert von: 252 — Fanny Kortüm,1 Soma Das,2 Max Flindt,1 Deborah J Morris-Rosendahl,3. Irina Stefanova,. 4. Amy Goldstein,. 5. Denise Horn,. 6. Eva Klopocki,. 6. Gerhard Kluger,.

6 - Northwestern Scholars

www.scholars.northwestern.edu

von V Shashi · · Zitiert von: 10 — ... Satu Korpi-Heikkilä, Olli Pietilainen, Palotie Aarno, Mitja I. Kurki, Alexander Hoischen, Anna C. Need, David B. Goldstein, Fanny Kortüm. › ...

De Novo Truncating Variants in ASXL2 Are Associated with a ...

www.academia.edu

... Mitja I. Kurki, Alexander Hoischen, Anna C. Need, David B. Goldstein, and Fanny Kortüm (The American Journal of Human Genetics 99, 991–999; October 6, ... › De_N...

De Novo Truncating Variants in ASXL2 Are Associated with ...Washington University in St. Louis

profiles.wustl.edu

von V Shashi · · Zitiert von: 62 — Goldstein, Fanny Kortüm Show 180 others. Show less. Division of Laboratory and Genomic Medicine · Institute of Clinical and Translational ...

De Novo Truncating Variants in ASXL2 Are Associated with a ...Elsevier

ohsu.elsevierpure.com

Goldstein, Fanny Kortüm Show 180 others. Show less. Research output: Contribution to journal › Article › peer-review. 53 Scopus citations. Overview ...

The core FOXG1 syndrome phenotype consists of postnatal microcephaly,...

experts.umn.edu

Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, ...

The core FOXG1 syndrome phenotype consists of postnatal ...

opus4.kobv.de

von F Kortüm · · Zitiert von: 230 — Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, ... › year › docId

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