Showing results (61-70 of 328) with videos related to
Sort By:
Pageof 33
Human Genetics|November 1, 1989
Diagnosis of genetic disease using recombinant DNA. Second editionD N Cooper, J SchmidtkeHuman Genetics|September 1, 1991
Diagnosis of genetic disease using recombinant DNA. Third editionD N Cooper, J SchmidtkeRadiology|October 1, 1984
Medullary nephrocalcinosis and pancreatic calcifications demonstrated by ultrasound and CT in infants after treatment with ACTHH P Rausch, F Hanefeld, H J KaufmannMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1987
[Mucolipidosis type II (I-cell disease) with unusually severe heart involvement]R Schulz, J Vogt, W Voss, et al.Neuropadiatrie|August 1, 1976
Protein patterns of the cerebrospinal fluid in children with cerebral palsyH Siemes, M Siegert, D Rating, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 13, 2007
Proton MRS of a child with Sandhoff disease reveals elevated brain hexosamineB Wilken, P Dechent, F Hanefeld, et al.Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|April 1, 1990
[Magnetic resonance tomography of laminar heterotopia]G Vahldiek, B Terwey, F Hanefeld, et al.HNO|August 28, 2003
[The Levy-Hollister syndrome: a syndrome of dysplasias with ENT-manifestations]O Fierek, R Laskawi, C Bönnemann, et al.Neurology|November 24, 2004
CSF characteristics in early-onset multiple sclerosisD Pohl, K Rostasy, H Reiber, et al.Human Mutation|March 10, 2001
Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regionsF Laccone, P Huppke, F Hanefeld, et al.Pageof 33