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H D Rott

Showing results (71-80 of 99) with videos related to

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Lancet (London, England)|January 20, 1996
Outcome of an enterohaemorrhagic Escherichia coli O157 infection in monozygotic twinsK Ludwig, H Ruder, H D Rott, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 1, 1991
Keratotorus in Norrie diseaseG E Lang, H D Rott, G O Naumann
Ophthalmic Paediatrics and Genetics|April 1, 1985
Observation concerning the age of onset and the nature of optic atrophy in Wolfram's syndrome (DIDMOADS)U M Mayer, H D Rott, H J Böhles
Journal of Neurology|February 1, 1987
Myotonic muscular dystrophy: structural changes visualized by ultrasoundW P Kaschka, K F Druschky, H D Rott
Genetic Counseling (Geneva, Switzerland)|October 28, 2003
Multiple malformations in a male and maternal osteopathia strata with cranial sclerosis (OSCS)H D Rott, P Krieg, H Rütschle, et al.
Journal De Genetique Humaine|September 1, 1984
Duchenne's muscular dystrophy: carrier detection by imaging technicsH D Rott, W Rödl, M Santellani, et al.
Klinische Padiatrie|November 1, 1978
[Spongious cerebral dystrophy at an infant age (Canavan-Bogaert-Bertrand types) in three siblings of a non-Jewish family in upper Franconia (author's transl)]H Schmidt, H D Rott, G Neuhäuser, et al.
Lancet (London, England)|November 19, 1983
Duchenne muscular dystrophy: carrier detection by ultrasound and computerised tomographyH D Rott, M Santellani, W Rödl, et al.
Human Genetics|July 12, 1978
Kartagener's syndrome in sibs: clinical and immunologic investigationsH D Rott, H Warnatz, R Pasch-Hilgers, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1971
[Mosaic Down's syndrome]K P Grosse, G Grosse, G Schwanitz, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
Lancet (London, England)|January 20, 1996
Outcome of an enterohaemorrhagic Escherichia coli O157 infection in monozygotic twinsK Ludwig, H Ruder, H D Rott, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 1, 1991
Keratotorus in Norrie diseaseG E Lang, H D Rott, G O Naumann
Ophthalmic Paediatrics and Genetics|April 1, 1985
Observation concerning the age of onset and the nature of optic atrophy in Wolfram's syndrome (DIDMOADS)U M Mayer, H D Rott, H J Böhles
Journal of Neurology|February 1, 1987
Myotonic muscular dystrophy: structural changes visualized by ultrasoundW P Kaschka, K F Druschky, H D Rott
Genetic Counseling (Geneva, Switzerland)|October 28, 2003
Multiple malformations in a male and maternal osteopathia strata with cranial sclerosis (OSCS)H D Rott, P Krieg, H Rütschle, et al.
Journal De Genetique Humaine|September 1, 1984
Duchenne's muscular dystrophy: carrier detection by imaging technicsH D Rott, W Rödl, M Santellani, et al.
Klinische Padiatrie|November 1, 1978
[Spongious cerebral dystrophy at an infant age (Canavan-Bogaert-Bertrand types) in three siblings of a non-Jewish family in upper Franconia (author's transl)]H Schmidt, H D Rott, G Neuhäuser, et al.
Lancet (London, England)|November 19, 1983
Duchenne muscular dystrophy: carrier detection by ultrasound and computerised tomographyH D Rott, M Santellani, W Rödl, et al.
Human Genetics|July 12, 1978
Kartagener's syndrome in sibs: clinical and immunologic investigationsH D Rott, H Warnatz, R Pasch-Hilgers, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1971
[Mosaic Down's syndrome]K P Grosse, G Grosse, G Schwanitz, et al.
Pageof 10