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H D Rott

Showing results (81-90 of 99) with videos related to

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Humangenetik|January 1, 1972
C 11-D 13-translocation in four generationsH D Rott, G Schwanitz, K P Grosse, et al.
Archiv Fur Gynakologie|January 1, 1972
[Chromosome studies in couples with repeated abortions]H D Rott, E Richter, W D Rummel, et al.
Deutsche Medizinische Wochenschrift (1946)|February 8, 1974
[The XXYY variant of Klinefelter's syndrome (author's transl)]O P Hornstein, H D Rott, G Schwanitz, et al.
Fortschritte Der Medizin|March 1, 1973
[Anticonvulsants and chromosome aberrations]K P Grosse, G Schwanitz, H D Rott, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1990
Hypomelanosis of Ito (incontinentia pigmenti achromians). Ophthalmological evidence for somatic mosaicismH D Rott, G E Lang, W Huk, et al.
Humangenetik|January 1, 1972
[Chromosome studies in persons treated with anticonvulsant drugs]K P Grosse, G Schwanitz, H D Rott, et al.
Journal of Medical Genetics|May 4, 2004
Characterisation of a novel TSC2 missense mutation in the GAP related domain associated with minimal clinical manifestations of tuberous sclerosisK Mayer, M Goedbloed, K van Zijl, et al.
Klinische Padiatrie|November 1, 1972
[E 18 ring chromosome--case report and review]K P Grosse, G Schwanitz, H D Rott, et al.
Clinical Genetics|August 1, 1992
A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)A Rauch, R A Pfeiffer, U Trautmann, et al.
Humangenetik|April 16, 1973
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case]M O Rethoré, H Hoehn, H D Rott, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Humangenetik|January 1, 1972
C 11-D 13-translocation in four generationsH D Rott, G Schwanitz, K P Grosse, et al.
Archiv Fur Gynakologie|January 1, 1972
[Chromosome studies in couples with repeated abortions]H D Rott, E Richter, W D Rummel, et al.
Deutsche Medizinische Wochenschrift (1946)|February 8, 1974
[The XXYY variant of Klinefelter's syndrome (author's transl)]O P Hornstein, H D Rott, G Schwanitz, et al.
Fortschritte Der Medizin|March 1, 1973
[Anticonvulsants and chromosome aberrations]K P Grosse, G Schwanitz, H D Rott, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1990
Hypomelanosis of Ito (incontinentia pigmenti achromians). Ophthalmological evidence for somatic mosaicismH D Rott, G E Lang, W Huk, et al.
Humangenetik|January 1, 1972
[Chromosome studies in persons treated with anticonvulsant drugs]K P Grosse, G Schwanitz, H D Rott, et al.
Journal of Medical Genetics|May 4, 2004
Characterisation of a novel TSC2 missense mutation in the GAP related domain associated with minimal clinical manifestations of tuberous sclerosisK Mayer, M Goedbloed, K van Zijl, et al.
Klinische Padiatrie|November 1, 1972
[E 18 ring chromosome--case report and review]K P Grosse, G Schwanitz, H D Rott, et al.
Clinical Genetics|August 1, 1992
A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)A Rauch, R A Pfeiffer, U Trautmann, et al.
Humangenetik|April 16, 1973
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case]M O Rethoré, H Hoehn, H D Rott, et al.
Pageof 10