Simone Schuffenhauer - Dokumente zum Namen

(1 - 13 von 13

)

Cyclic GMP contact points within the 63-kDa subunit and a 240-kDa ...pubs.acs.org › doi

pubs.acs.org

· Nature Genetics 1998, 19 (3) , https://doi.org ; Bernd Wissinger, Frank Müller, Ingo Weyand, Simone Schuffenhauer, ...

A familial deletion in the Prader‐Willi syndrome region including the ...onlinelibrary.wiley.com › doi

onlinelibrary.wiley.com

Simone Schuffenhauer,. Simone Schuffenhauer. Abteilung Pädiatrische Genetik, Kinderpoliklinik, Ludwig-Maximilians-Universität, D München, Germany.

Simone Schuffenhauer - Academia.edu

independent.academia.edu

› ...

The Mouse Pink‐Eyed Dilution Gene: Association with ...onlinelibrary.wiley.com › doi › abs › j

onlinelibrary.wiley.com

SIMONE SCHUFFENHAUER. Abteilung für Pädiatrische Genetik der Kinderpoliklinik der Universität München, München, Germany.

DeepDyve - Unlimited Access to Peer-Reviewed Journals

www.deepdyve.com

DeepDyve is the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.

Craniosynostosis suggestive of Saethre-Chotzen syndrome: Clinical...

pdfslide.net

American Journal of Medical Genetics 63: (1996) Craniosynostosis Suggestive of Saethre-Chotzen Syndrome: Clinical Description of a Large Kindred and Exclusion of Candidate Regions on 7p Steven von Gernet, Simone Schuffenhauer, Astrid Golla, Peter Lichtner, Stefanie Balg, Wolfgang ...

Focus on holoprosencephaly By Deepak Kamnasaran A t - ERA

era.library.ualberta.ca

von D Kamnasaran · — Quarrell (Sheffield Children's Hospital, UK), Simone Schuffenhauer (Ludwig-. Maximilians University Munich, Germany), Jennifer Gerritsen (Alberta Children. › items › download

Phenotypic expression ofthe fibroblast growth factor receptor

search.proquest.com

von A Golla · · Zitiert von: 53 — large craniosynostosis family. Astrid Golla, Peter Lichtner, Steven von Gernet, Andreas Winterpacht, Jeffrey Fairley,. Jan Murken, Simone Schuffenhauer. › openview › 1.pdf

[PDF] Mikrodeletionen als Ursache pädiatrischer Krankheitsbilderwww.medgenetik.de › 2001_2_117_Schuffenhauer

www.medgenetik.de

Simone Schuffenhauer', Dieter Kotzot². 1) Abteilung Medizinische Genetik,. Kinderklinik, LMU München,. 2) Institut für Humangenetik,. TU München.

[PDF] Toward Global Biobank Integration by Implementation of the ...research.rug.nl › files › Toward_Global_Biobank_Integration_by_Im...

research.rug.nl

Simone Schuffenhauer,4 Kaisa Silander,5 Linda Mook,2 Petr Holub,6. Raffael Bild,7 Morris Swertz,2 and Jan-Eric Litton6. Biobanks are the biological back end ...