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G Schwanitz

Showing results (71-80 of 123) with videos related to

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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.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1984
Klinefelter's syndrome and mitral valve prolapse. an echocardiographic study in twenty-two patientsG R Fricke, H J Mattern, H U Schweikert, et al.
Klinische Padiatrie|February 28, 2001
[Bardet-Biedl syndrome: aspects of nephro-urology and human genetics]P Brühl, G Schwanitz, R Mallmann, et al.
Clinical Genetics|August 1, 1997
Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissuesS Rudnik-Schöneborn, R Schubert, F Majewski, et al.
Fortschritte Der Medizin|March 1, 1973
[Anticonvulsants and chromosome aberrations]K P Grosse, G Schwanitz, H D Rott, et al.
Human Genetics|April 1, 1997
Molecular investigation of the parental origin of a de novo unbalanced translocation 13/18T Eggermann, H Engels, C Heidrich-Kaul, et al.
Humangenetik|January 1, 1972
[Chromosome studies in persons treated with anticonvulsant drugs]K P Grosse, G Schwanitz, H D Rott, et al.
Genomics|June 15, 1996
Localization of the human glucosidase I gene to chromosome 2p12-p13 by fluorescence in situ hybridization and PCR analysis of somatic cell hybridsB Kalz-Füller, C Heidrich-Kaul, M Nöthen, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|October 18, 2000
Combination of hypospadias and maldescended testis as cardinal symptoms in gonosomal chromosome aberrationsR Raff, R Schubert, G Schwanitz, et al.
Pageof 13

Showing results (71-80 of 123) with videos related to

Sort By:
Pageof 13
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.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1984
Klinefelter's syndrome and mitral valve prolapse. an echocardiographic study in twenty-two patientsG R Fricke, H J Mattern, H U Schweikert, et al.
Klinische Padiatrie|February 28, 2001
[Bardet-Biedl syndrome: aspects of nephro-urology and human genetics]P Brühl, G Schwanitz, R Mallmann, et al.
Clinical Genetics|August 1, 1997
Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissuesS Rudnik-Schöneborn, R Schubert, F Majewski, et al.
Fortschritte Der Medizin|March 1, 1973
[Anticonvulsants and chromosome aberrations]K P Grosse, G Schwanitz, H D Rott, et al.
Human Genetics|April 1, 1997
Molecular investigation of the parental origin of a de novo unbalanced translocation 13/18T Eggermann, H Engels, C Heidrich-Kaul, et al.
Humangenetik|January 1, 1972
[Chromosome studies in persons treated with anticonvulsant drugs]K P Grosse, G Schwanitz, H D Rott, et al.
Genomics|June 15, 1996
Localization of the human glucosidase I gene to chromosome 2p12-p13 by fluorescence in situ hybridization and PCR analysis of somatic cell hybridsB Kalz-Füller, C Heidrich-Kaul, M Nöthen, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|October 18, 2000
Combination of hypospadias and maldescended testis as cardinal symptoms in gonosomal chromosome aberrationsR Raff, R Schubert, G Schwanitz, et al.
Pageof 13