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Christian Hafner

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The Journal of Investigative Dermatology|April 23, 2016

Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal NeviAgustí Toll, Luis C Fernández, Tirso Pons, et al.

Nature Communications|February 11, 2018

Genetic alterations driving metastatic colony formation are acquired outside of the primary tumour in melanomaMelanie Werner-Klein, Sebastian Scheitler, Martin Hoffmann, et al.

American Journal of Human Genetics|January 7, 2014

Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos diseaseF Buket Basmanav, Ana-Maria Oprisoreanu, Sandra M Pasternack, et al.

American Journal of Human Genetics|May 31, 2016

A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones SyndromeStephen R F Twigg, Robert B Hufnagel, Kerry A Miller, et al.

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Search research articles

Showing results (111-120 of 114) with videos related to

Sort By:

Pageof 12

You have reached the last page of results.This site can display upto 114 results.

The Journal of Investigative Dermatology|April 23, 2016

Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal NeviAgustí Toll, Luis C Fernández, Tirso Pons, et al.

Nature Communications|February 11, 2018

Genetic alterations driving metastatic colony formation are acquired outside of the primary tumour in melanomaMelanie Werner-Klein, Sebastian Scheitler, Martin Hoffmann, et al.

American Journal of Human Genetics|January 7, 2014

Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos diseaseF Buket Basmanav, Ana-Maria Oprisoreanu, Sandra M Pasternack, et al.

American Journal of Human Genetics|May 31, 2016

A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones SyndromeStephen R F Twigg, Robert B Hufnagel, Kerry A Miller, et al.

Pageof 12