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HNO|June 1, 1980
[Genetically determinded deafness; 5 cases of Pendred's syndrome (author's transl)]K Hörmann, K R HeldMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1981
[Growth and nutrition: long term follow-up in early treated phenylketonuric and hyperphenylalaninemic children (author's transl)]P Koepp, G Hinze, K R HeldPediatric Radiology|April 1, 1980
Mesomelic dysplasia with short ulna, long fibula, brachymetacarpy, and micrognathia. Clinical and radiological differential diagnostic featuresU Burck, E Schaefer, K R HeldGenetics|December 1, 1974
The locus for human adenine phosphoribosyltransferase on chromosome no. 16B Kahan, K R Held, R DeMarsClinical Genetics|November 27, 1998
Presence of the AZF region in a female with an idic(Y)(q11)J Jenderny, W Schmidt, K R HeldHumangenetik|October 20, 1975
Adenine phosphoribosyltransferase and hypoxanthine-guanine phosphoribosyltransferase immunoprecipitation reactions in human-mouse and human-hamster cell hybridsK R Held, B Kahan, R DeMarsClinical Genetics|September 1, 1986
Dermatoglyphics in congenital adrenal hyperplasia (CAH)D Börger, K R Held, S LüttgenKlinische Monatsblatter Fur Augenheilkunde|July 1, 1983
[Congenital malformations in the area of the eye and their significance in the diagnosis of major syndromes and in genetic counseling]U Burck, J Brönneke, K R HeldCochlear Implants International|September 16, 2011
Towards quantifying cochlear implant localization performance in complex acoustic environmentsS Kerber, B U SeeberAmerican Journal of Medical Genetics|April 1, 1982
Occurrence of cyclopia, myelomeningocele, deafness, and abducens paralysis in siblingsU Burck, K R Held, H J KitschkePageof 11