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European Journal of Pediatrics|January 1, 1987
An unusual, possibly "new" MA/MR syndrome with sagittal craniosynostosisR A Pfeiffer, U Tietze, W WelteJournal of Medical Genetics|February 1, 1977
46,XX/46,XX,r(15) mosaiciam: report of a caseR A Pfeiffer, R Dhadial, W LenzJournal of Physics. Condensed Matter : an Institute of Physics Journal|October 4, 2018
Importance of spin current generation and detection by spin injection and the spin Hall effect for lateral spin valve performanceA Pfeiffer, R M Reeve, M KläuiJournal De Genetique Humaine|March 1, 1979
[Familial translocation 22/Y and partial autosomal trisomy in a young girl]E Kessel, R A Pfeiffer, P WellingKlinische Padiatrie|May 1, 1976
[The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)]E Kessel, R A Pfeiffer, W KosenowKlinische Padiatrie|January 1, 1980
[Postaxial polydactyly: a symptom of partial trisomy of the long arm of chromosome 13. Two new observations with 46, XX, t (22;13) (q13;q31) and 46, XY, Dup (13) (pter-q34::q22-qter) (author's transl)]E Kessel, R A Pfeiffer, C BaischPediatric Radiology|January 1, 1992
An autosomal recessive variant of spondylo-epiphyseal dysplasia in three sibsR A Pfeiffer, J Suess, M HaagenHelvetica Paediatrica Acta|September 1, 1977
[The Schwartz-Jampel syndrome (myotonia chondrodystrophica)]R A Pfeiffer, H Bauer, C PetersenNaunyn-Schmiedeberg'S Archives of Pharmacology|November 3, 1975
Muscarinic inhibition of potassium-induced noradrenaline release and its dependence on the calcium concentrationM P Dubey, E Muscholl, A PfeifferClinical Genetics|August 1, 1992
Typical and partial cat eye syndrome: identification of the marker chromosome by FISHT Liehr, R A Pfeiffer, U TrautmannPageof 90