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Journal Article
BMC Medical Genetics, ISSN 1471-2350, 12/2012, Volume 13, Issue 1, pp. 123 - 123
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, pp. e93607 - e93607
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2011, Volume 88, Issue 6, pp. 852 - 860
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 1/2008, Volume 17, Issue 2, pp. 256 - 265
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 05/2018, Volume 52, Issue 9, p. 599
BackgroundKeratosis pilaris atrophicans (KPA) is a group of rare genodermatoses characterised by perifollicular keratosis and inflammation that progresses to... 
Journal Article
Stem Cell Research, ISSN 1873-5061, 08/2019, Volume 39, pp. 101518 - 101518
Mowat-Wilson syndrome (MWS) is a complex developmental syndrome caused by heterozygous mutations in the Zinc finger E-box-binding homeobox 2 gene ( ). We... 
Index Medicus
Journal Article
Archives of Dermatological Research, ISSN 0340-3696, 7/2012, Volume 304, Issue 5, pp. 377 - 386
Journal Article