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HNO|October 17, 1998
[Small abnormality of the middle ear--a genetically-induced defect?]C Thies, K Sperling, A Reis, et al.Journal of Medical Genetics|July 1, 1996
Possible autosomal recessive inheritance of progressive hearing loss with stapes fixationC Thies, M Handrock, K Sperling, et al.Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|August 10, 1999
Nijmegen breakage syndrome: consequences of defective DNA double strand break repairM Digweed, A Reis, K SperlingHuman Genetics|September 1, 1992
Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12-q21A Reis, W Küster, R Eckardt, et al.American Journal of Medical Genetics|December 11, 1996
Phenotypic differences in Angelman syndrome patients: imprinting mutations show less frequently microcephaly and hypopigmentation than deletionsJ Bürger, J Kunze, K Sperling, et al.Laryngologie, Rhinologie, Otologie|October 1, 1978
[Reaction pattern of the cochlea in cases of experimentally induced sudden hearing loss (author's transl)]M HandrockLaryngologie, Rhinologie, Otologie|May 1, 1979
["Sudden binaural deafness" after acute heroin intoxication (author's transl)]G Mulch, M HandrockArchives of Oto-Rhino-Laryngology|January 1, 1982
The influence of the effect system on adaptation, temporary and permanent threshold shiftM Handrock, J ZeisbergLaryngologie, Rhinologie, Otologie|August 1, 1976
[The significance of IgE in the differential diagnosis of vasomotoric rhinopathy (author's transl)]M Handrock, A BaumgärtelHNO|December 5, 2000
[Functional and esthetic results of osteoplastic frontal sinus operations and profile reconstruction with bitemporal coronal incision]I Kausch, M HandrockPageof 123