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European Journal of Endocrinology|October 11, 2007
Genetic disorders in the GH IGF-I axis in mouse and manM J E Walenkamp, J M Wit
Hormone Research|August 19, 2006
Genetic disorders in the growth hormone - insulin-like growth factor-I axisM J E Walenkamp, J M Wit
Endocrine Development|February 9, 2013
Molecular IGF-1 and IGF-1 receptor defects: from genetics to clinical managementM J E Walenkamp, M Losekoot, J M Wit
Annals of Human Biology|September 10, 2003
Adult height corrected for shrinking and secular trendR Niewenweg, M L Smit, M J E Walenkamp, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 23, 2009
A case of premature thelarche with no central cause or genetic variants within the estrogen receptor signaling pathwayR J Hartmaier, M J E Walenkamp, A S Richter, et al.
Hormone Research in Paediatrics|December 17, 2013
Genetic analysis of GHR should contain sequencing of all coding exons and specific intron sequences, and screening for exon deletionsM J E Walenkamp, J Klammt, E Feigerlova, et al.
European Journal of Medical Genetics|October 24, 2006
Tall stature and duplication of the insulin-like growth factor I receptor geneS G Kant, M Kriek, M J E Walenkamp, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2006
A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptorM J E Walenkamp, H J van der Kamp, A M Pereira, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|January 18, 2011
The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated proteinH A van Duyvenvoorde, J van Doorn, J Koenig, et al.
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