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H D Rott

Showing results (41-50 of 99) with videos related to

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Humangenetik|January 1, 1973
The effect of ultrasound on human chromosomes in vitroH D Rott, R Soldner
Munchener Medizinische Wochenschrift (1950)|May 28, 1971
[Dermatoglyphic disorders in rubella embryopathy]H D Rott, H Jolk
Journal De Genetique Humaine|October 1, 1982
[Absence of fre(X)q27/q28 in the X-linked microcephaly syndrome]C Faschingbauer, H D Rott
Acta Geneticae Medicae Et Gemellologiae|January 1, 1973
[Cytogenetic studies on the seasonal variations in the rate of spontaneous chromosomal aberrations in man]B R Deininger, H D Rott
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 1, 1974
[Nuclear sex diagnosis using hair root cells]H D Rott, O P Hornstein
Human Mutation|June 30, 2000
Tuberous sclerosis type 1: three novel mutations detected in exon 15 by a combination of HDA and TGGEJ Hass, K Mayer, H D Rott
Monatsschrift Fur Kinderheilkunde|July 1, 1970
[Partial trisomy E18 (E18 q--) due to a balanced translocation D-E in the mother]M Gleissner, G Schwanitz, H D Rott
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1982
[A rare form of optical, choroidal and retinal dysplasia combined with an occipital encephalocele]U Mayer, M Klinger, H D Rott
Human Genetics|November 1, 1991
A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locusR Fahsold, H D Rott, P Lorenz
Der Nervenarzt|January 1, 1982
[Cerebral calcifications in a patient with tuberous sclerosis without convulsions (author's transl)]H D Rott, W Huk, E Müller
Pageof 10

Showing results (41-50 of 99) with videos related to

Sort By:
Pageof 10
Humangenetik|January 1, 1973
The effect of ultrasound on human chromosomes in vitroH D Rott, R Soldner
Munchener Medizinische Wochenschrift (1950)|May 28, 1971
[Dermatoglyphic disorders in rubella embryopathy]H D Rott, H Jolk
Journal De Genetique Humaine|October 1, 1982
[Absence of fre(X)q27/q28 in the X-linked microcephaly syndrome]C Faschingbauer, H D Rott
Acta Geneticae Medicae Et Gemellologiae|January 1, 1973
[Cytogenetic studies on the seasonal variations in the rate of spontaneous chromosomal aberrations in man]B R Deininger, H D Rott
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 1, 1974
[Nuclear sex diagnosis using hair root cells]H D Rott, O P Hornstein
Human Mutation|June 30, 2000
Tuberous sclerosis type 1: three novel mutations detected in exon 15 by a combination of HDA and TGGEJ Hass, K Mayer, H D Rott
Monatsschrift Fur Kinderheilkunde|July 1, 1970
[Partial trisomy E18 (E18 q--) due to a balanced translocation D-E in the mother]M Gleissner, G Schwanitz, H D Rott
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1982
[A rare form of optical, choroidal and retinal dysplasia combined with an occipital encephalocele]U Mayer, M Klinger, H D Rott
Human Genetics|November 1, 1991
A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locusR Fahsold, H D Rott, P Lorenz
Der Nervenarzt|January 1, 1982
[Cerebral calcifications in a patient with tuberous sclerosis without convulsions (author's transl)]H D Rott, W Huk, E Müller
Pageof 10