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Humangenetik|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 HeldAmerican Journal of Medical Genetics|April 1, 1982
Occurrence of cyclopia, myelomeningocele, deafness, and abducens paralysis in siblingsU Burck, K R Held, H J KitschkeAmerican Journal of Medical Genetics|January 1, 1990
Clinical pattern and the genetics of the fetal iodine deficiency disorder (endemic cretinism): results of a field study in Highland EcuadorK R Held, M E Cruz, F MoncayoGeburtshilfe Und Frauenheilkunde|September 1, 1981
[Prenatal sex determination via GBN saliva test. A comparison with the results of prenatal chromosomal analysis]K R Held, U Burck, T Koske-WestphalHuman Genetics|January 1, 1996
Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4XC Geerkens, W Just, K R Held, et al.Annals of Nutrition & Metabolism|January 1, 1983
Plasma amino acid pattern at noon in early treated hyperphenylalaninemic, phenylketonuric, and normal childrenK R Held, P Koepp, C Plettner, et al.Helvetica Paediatrica Acta|November 1, 1981
Bilateral femoral dysgenesis with micrognathia, cleft palate, anomalies of the spine and pelvis, and foot deformities. Clinical and radiological findingsU Burck, T Riebel, K R Held, et al.Human Genetics|May 1, 1992
Expression of RPS4X in fibroblasts from patients with structural aberrations of the X chromosomeW Just, C Geerkens, K R Held, et al.Pageof 4