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Human Genetics
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November 1, 1994
Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma
V Greger, N Debus, D Lohmann, et al.
Sensors (Basel, Switzerland)
|
February 10, 2024
Compact and Fully Integrated LED Quantum Sensor Based on NV Centers in Diamond
Jens Pogorzelski, Ludwig Horsthemke, Jonas Homrighausen, et al.
Journal of Medical Genetics
|
April 5, 2005
Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples
M Ludwig, A Katalinic, S Gross, et al.
American Journal of Human Genetics
|
April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndrome
K Buiting, A Barnicoat, C Lich, et al.
Plos One
|
September 11, 2013
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1
Laura Steenpass, Deniz Kanber, Michaela Hiber, et al.
Sensors (Basel, Switzerland)
|
May 25, 2024
Microcontroller-Optimized Measurement Electronics for Coherent Control Applications of NV Centers
Dennis Stiegekötter, Jens Pogorzelski, Ludwig Horsthemke, et al.
European Journal of Biochemistry
|
April 1, 1987
Unequal crossing-over between two alu-repetitive DNA sequences in the low-density-lipoprotein-receptor gene. A possible mechanism for the defect in a patient with familial hypercholesterolaemia
B Horsthemke, U Beisiegel, A Dunning, et al.
Cytogenetics and Cell Genetics
|
September 8, 1998
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes
K Buiting, S Gross, Y Ji, et al.
Cytogenetic and Genome Research
|
July 18, 2018
Angelman Syndrome-Affected Individual with a Numerically Normal Karyotype and Isodisomic Paternal Uniparental Disomy of Chromosome 15 due to Maternal Robertsonian Translocation (14;15) by Monosomy Rescue
Nuria C Bramswig, Karin Buiting, Natalie Bechtel, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2011
Automated syndrome detection in a set of clinical facial photographs
Stefan Boehringer, Manuel Guenther, Stella Sinigerova, et al.
Page
of 37
Search research articles
Search
Showing results (181-190 of 368) with videos related to
Sort By:
Page
of 37
Human Genetics
|
November 1, 1994
Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma
V Greger, N Debus, D Lohmann, et al.
Sensors (Basel, Switzerland)
|
February 10, 2024
Compact and Fully Integrated LED Quantum Sensor Based on NV Centers in Diamond
Jens Pogorzelski, Ludwig Horsthemke, Jonas Homrighausen, et al.
Journal of Medical Genetics
|
April 5, 2005
Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples
M Ludwig, A Katalinic, S Gross, et al.
American Journal of Human Genetics
|
April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndrome
K Buiting, A Barnicoat, C Lich, et al.
Plos One
|
September 11, 2013
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1
Laura Steenpass, Deniz Kanber, Michaela Hiber, et al.
Sensors (Basel, Switzerland)
|
May 25, 2024
Microcontroller-Optimized Measurement Electronics for Coherent Control Applications of NV Centers
Dennis Stiegekötter, Jens Pogorzelski, Ludwig Horsthemke, et al.
European Journal of Biochemistry
|
April 1, 1987
Unequal crossing-over between two alu-repetitive DNA sequences in the low-density-lipoprotein-receptor gene. A possible mechanism for the defect in a patient with familial hypercholesterolaemia
B Horsthemke, U Beisiegel, A Dunning, et al.
Cytogenetics and Cell Genetics
|
September 8, 1998
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes
K Buiting, S Gross, Y Ji, et al.
Cytogenetic and Genome Research
|
July 18, 2018
Angelman Syndrome-Affected Individual with a Numerically Normal Karyotype and Isodisomic Paternal Uniparental Disomy of Chromosome 15 due to Maternal Robertsonian Translocation (14;15) by Monosomy Rescue
Nuria C Bramswig, Karin Buiting, Natalie Bechtel, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2011
Automated syndrome detection in a set of clinical facial photographs
Stefan Boehringer, Manuel Guenther, Stella Sinigerova, et al.
Page
of 37