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American Journal of Medical Genetics|June 24, 1998
A rare form of spondylometaphyseal dysplasia-type A4T Duetting, A Schulze, J Troeger, et al.Radiology|February 1, 1975
The Dyggve-Melchior-Clausen syndromeJ Spranger, P Maroteaux, V M Der KaloustianSkeletal Radiology|January 1, 1982
Wormian bones in osteogenesis imperfecta and other disordersB Cremin, H Goodman, J Spranger, et al.Journal of Neurology|August 4, 1975
[The occurrence of diabetes mellitus, diabetes insipidus, optic atrophy and neurogenic deafness in one patient (author's transl)]K Foerster, J Spranger, J Beyer, et al.American Journal of Medical Genetics. Part A|February 11, 2005
Escobar variant with pursed mouth, creased tongue, ophthalmologic features, and scoliosis in 6 children from OmanAnna Rajab, K Hoffmann, A Ganesh, et al.Development (Cambridge, England)|December 1, 1993
Nuclear localization of the protein encoded by the Wilms' tumor gene WT1 in embryonic and adult tissuesS Mundlos, J Pelletier, A Darveau, et al.European Journal of Human Genetics : EJHG|March 28, 2008
Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor geneS Türkmen, K Hoffmann, Osman Demirhan, et al.Genomics|October 27, 1998
Characterization of a human homologue of the Saccharomyces cerevisiae transcription factor spt3 (SUPT3H)J Yu, J M Madison, S Mundlos, et al.Clinical Genetics|March 27, 2009
Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3B Tuysuz, S Mizumoto, K Sugahara, et al.Diabetes|September 1, 1997
Growth factor alterations in advanced diabetic retinopathy: a possible role of blood retina barrier breakdownA Pfeiffer, J Spranger, R Meyer-Schwickerath, et al.Pageof 23