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Ute Grasshoff

Showing results (1-10 of 45) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|August 29, 2023
An early onset cone dystrophy due to CEP290 mutation: a case reportAnastasia Binder, Susanne Kohl, Ute Grasshoff, et al.
Frontiers in Neurology|February 26, 2021
The Role of Neuroimaging and Genetic Analysis in the Diagnosis of Children With Cerebral PalsyVeronka Horber, Ute Grasshoff, Elodie Sellier, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Interstitial 3p25.3-p26.1 deletion in a patient with intellectual disabilityAngelika Riess, Ute Grasshoff, Karin Schäferhoff, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 6, 2018
Further evidence for complex inheritance of holoprosencephaly: Lessons learned from pre- and postnatal diagnostic testing in GermanySophie Hinreiner, Dagmar Wieczorek, Dietmar Mueller, et al.
American Journal of Medical Genetics. Part A|March 23, 2013
Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disabilityAnastasia Gazou, Angelika Riess, Ute Grasshoff, et al.
American Journal of Medical Genetics. Part A|April 25, 2013
12q24.33 deletion: report of a patient with intellectual disability and review of the literatureMartin Kehrer, Sylke Singer, Ute Grasshoff, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Interstitial duplication of chromosome region 1q25.1q25.3: report of a patient with mild cognitive deficits, tall stature and facial dysmorphismsMartin Kehrer, Thomas Liehr, Tanja Benkert, et al.
Journal of Medical Genetics|July 31, 2012
Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literatureMatthias Begemann, Sabrina Spengler, Magdalena Gogiel, et al.
American Journal of Medical Genetics. Part A|May 29, 2012
Interstitial 9q34.11-q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palateAndreas Tzschach, Ute Grasshoff, Karin Schäferhoff, et al.
Neurobiology of Aging|December 5, 2013
Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron diseaseMatthis Synofzik, Christoph Born, Axel Rominger, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Documenta Ophthalmologica. Advances in Ophthalmology|August 29, 2023
An early onset cone dystrophy due to CEP290 mutation: a case reportAnastasia Binder, Susanne Kohl, Ute Grasshoff, et al.
Frontiers in Neurology|February 26, 2021
The Role of Neuroimaging and Genetic Analysis in the Diagnosis of Children With Cerebral PalsyVeronka Horber, Ute Grasshoff, Elodie Sellier, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Interstitial 3p25.3-p26.1 deletion in a patient with intellectual disabilityAngelika Riess, Ute Grasshoff, Karin Schäferhoff, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 6, 2018
Further evidence for complex inheritance of holoprosencephaly: Lessons learned from pre- and postnatal diagnostic testing in GermanySophie Hinreiner, Dagmar Wieczorek, Dietmar Mueller, et al.
American Journal of Medical Genetics. Part A|March 23, 2013
Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disabilityAnastasia Gazou, Angelika Riess, Ute Grasshoff, et al.
American Journal of Medical Genetics. Part A|April 25, 2013
12q24.33 deletion: report of a patient with intellectual disability and review of the literatureMartin Kehrer, Sylke Singer, Ute Grasshoff, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Interstitial duplication of chromosome region 1q25.1q25.3: report of a patient with mild cognitive deficits, tall stature and facial dysmorphismsMartin Kehrer, Thomas Liehr, Tanja Benkert, et al.
Journal of Medical Genetics|July 31, 2012
Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literatureMatthias Begemann, Sabrina Spengler, Magdalena Gogiel, et al.
American Journal of Medical Genetics. Part A|May 29, 2012
Interstitial 9q34.11-q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palateAndreas Tzschach, Ute Grasshoff, Karin Schäferhoff, et al.
Neurobiology of Aging|December 5, 2013
Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron diseaseMatthis Synofzik, Christoph Born, Axel Rominger, et al.
Pageof 5