P M Kroisel - JoVE Visualize

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Clinical Genetics|April 19, 2003

Molecular characterization of a unique de novo 15q deletion associated with Prader-Willi syndrome and central visual impairmentC Windpassinger, E Petek, K Wagner, et al.

American Journal of Medical Genetics|June 26, 2001

Candidate region for Gilles de la Tourette syndrome at 7q31P M Kroisel, E Petek, W Emberger, et al.

Clinical Dysmorphology|April 20, 2001

Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter)E Petek, G Köstl, L Rauter, et al.

Journal of Medical Genetics|May 5, 1999

Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: first application on 247 chorionic villus samplesB Pertl, S Kopp, P M Kroisel, et al.

Human Genetics|July 1, 1996

Rapid detection of trisomies 21 and 18 and sexing by quantitative fluorescent multiplex PCRB Pertl, U Weitgasser, S Kopp, et al.

Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 5, 2002

[Psoriasis and hypogonadism in chronic blepharokeratoconjunctivitis. A case report]J Horwath-Winter, I Flögel, S Ramschak-Schwarzer, et al.

American Journal of Obstetrics and Gynecology|November 25, 1997

Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sexB Pertl, S Kopp, P M Kroisel, et al.

Genetic Counseling (Geneva, Switzerland)|July 23, 2003

Characterisation of a 19-year-old "long-term survivor" with Edwards syndromeE Petek, B Pertl, M Tschernigg, et al.

Cancer Genetics and Cytogenetics|August 25, 2001

Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;10;22)(q34;q22;q11)W Emberger, A Behmel, M Tschernigg, et al.

Journal of Medical Genetics|March 10, 2009

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testingT Schwarzbraun, A C Obenauf, A Langmann, et al.

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Showing results (21-30 of 37) with videos related to

Sort By:

Pageof 4

Clinical Genetics|April 19, 2003

Molecular characterization of a unique de novo 15q deletion associated with Prader-Willi syndrome and central visual impairmentC Windpassinger, E Petek, K Wagner, et al.

American Journal of Medical Genetics|June 26, 2001

Candidate region for Gilles de la Tourette syndrome at 7q31P M Kroisel, E Petek, W Emberger, et al.

Clinical Dysmorphology|April 20, 2001

Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter)E Petek, G Köstl, L Rauter, et al.

Journal of Medical Genetics|May 5, 1999

Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: first application on 247 chorionic villus samplesB Pertl, S Kopp, P M Kroisel, et al.

Human Genetics|July 1, 1996

Rapid detection of trisomies 21 and 18 and sexing by quantitative fluorescent multiplex PCRB Pertl, U Weitgasser, S Kopp, et al.

Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 5, 2002

[Psoriasis and hypogonadism in chronic blepharokeratoconjunctivitis. A case report]J Horwath-Winter, I Flögel, S Ramschak-Schwarzer, et al.

American Journal of Obstetrics and Gynecology|November 25, 1997

Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sexB Pertl, S Kopp, P M Kroisel, et al.

Genetic Counseling (Geneva, Switzerland)|July 23, 2003

Characterisation of a 19-year-old "long-term survivor" with Edwards syndromeE Petek, B Pertl, M Tschernigg, et al.

Cancer Genetics and Cytogenetics|August 25, 2001

Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;10;22)(q34;q22;q11)W Emberger, A Behmel, M Tschernigg, et al.

Journal of Medical Genetics|March 10, 2009

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testingT Schwarzbraun, A C Obenauf, A Langmann, et al.

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