Skip to main content


Page 4 of 4

  1. Authors: Jan Marquard, Silke Otter, Alena Welters, Diran Herebian, Fatih Demir, Annett Schroeter, Olaf Kletke, Martin Kragl, Daniel Eberhard, Barbara Bartosinska, Masa Skelin Klemen, Andraz Stozer, Martin Köhler, Alin Stirban, Freimut Schliess, Tim Heise…

    Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A26

    Content type: Meeting abstract

    Published on:

    This article is part of a Supplement: Volume 1 Supplement 1

  2. Congenital leptin deficiency is a rare autosomal recessive monogenic obesity syndrome caused by mutations in the leptin gene. This review describes the molecular and cellular characteristics of the eight disti...

    Authors: Jan-Bernd Funcke, Julia von Schnurbein, Belinda Lennerz, Georgia Lahr, Klaus-Michael Debatin, Pamela Fischer-Posovszky and Martin Wabitsch

    Citation: Molecular and Cellular Pediatrics 2014 1:3

    Content type: Review

    Published on:

  3. Fragile X is the most common form of inherited intellectual disability and the leading known genetic cause of autism. There is currently no cure or approved medication for fragile X although various drugs targ...

    Authors: Cara J Westmark

    Citation: Molecular and Cellular Pediatrics 2014 1:1

    Content type: Mini review

    Published on: