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Deutsche Medizinische Wochenschrift (1946)|July 2, 1982
[Improvement in the longitudinal growth in Ullrich-Turner syndrome with oxandrolone. Function of urinary excretion of steroid hormones]W Schönberger, P Benes, B Morsches, et al.
Klinische Padiatrie|May 1, 1992
[Clinical importance of hepatitis B virus DNA detection in serum of children with chronic hepatitis B]S Wirth, U Möllers, E Schaefer, et al.
Journal of Medical Genetics|January 8, 2008
A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndromeE Klopocki, C-E Ott, N Benatar, et al.
Nature Genetics|April 1, 1993
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectA Winterpacht, M Hilbert, U Schwarze, et al.
The Journal of Biological Chemistry|January 27, 1995
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilageD Chan, W G Cole, C W Chow, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 1, 1997
Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant miceL F Huang, N Fukai, P B Selby, et al.
Genomics|December 10, 1999
Isolation, characterization, and mapping of a zinc finger gene, ZFP95, containing both a SCAN box and an alternatively spliced KRAB A domainS D Dreyer, Q Zheng, B Zabel, et al.
The International Journal of Developmental Biology|December 1, 1996
Developmental expression of splicing variants of fibroblast growth factor receptor 3 (FGFR3) in mouseC Wuechner, A C Nordqvist, A Winterpacht, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
A disorder resembling pseudoachondroplasia but without COMP mutationJ W Spranger, B Zabel, J Kennedy, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 17, 2017
A novel COL1A2 C-propeptide cleavage site mutation causing high bone mass osteogenesis imperfecta with a regional distribution patternT Rolvien, U Kornak, J Stürznickel, et al.
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