Search research articles
Contact Us
Filters
Showing results (221-230 of 305) with videos related to
Page
of 31
Sort By:
BMC Medical Genetics
|
May 7, 2015
A novel large deletion of the ICR1 region including H19 and putative enhancer elements
Helen Fryssira, Stella Amenta, Deniz Kanber, et al.
Journal of Medical Genetics
|
October 1, 1996
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome
B Horsthemke, A Maat-Kievit, E Sleegers, et al.
Journal of Medical Ethics
|
March 27, 2010
Dutch experience of monitoring active ending of life for newborns
Hilde M Buiting, Maartje A C Karelse, Hens A A Brouwers, et al.
American Journal of Human Genetics
|
February 11, 1999
Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation
T Ohta, K Buiting, H Kokkonen, et al.
Human Molecular Genetics
|
February 9, 1999
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities
Y Ji, M J Walkowicz, K Buiting, et al.
Acta Diabetologica
|
October 16, 2014
Cobalamin status and its relation with depression, cognition and neuropathy in patients with type 2 diabetes mellitus using metformin
Elke Biemans, Huberta E Hart, Guy E H M Rutten, et al.
American Journal of Human Genetics
|
December 1, 1999
A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?
K Buiting, B Dittrich, B Dworniczak, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 23, 1996
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations
S Saitoh, K Buiting, P K Rogan, et al.
Molecular Cytogenetics
|
October 3, 2014
Partial and complete trisomy 14 mosaicism: clinical follow-up, cytogenetic and molecular analysis
Consuelo Salas-Labadía, Esther Lieberman, Roberto Cruz-Alcívar, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
August 5, 2018
Spatial clustering and livestock exposure as risk factor for community-acquired Clostridium difficile infection
S M van Dorp, M P M Hensgens, O M Dekkers, et al.
Page
of 31
Search research articles
Search
Showing results (221-230 of 305) with videos related to
Sort By:
Page
of 31
BMC Medical Genetics
|
May 7, 2015
A novel large deletion of the ICR1 region including H19 and putative enhancer elements
Helen Fryssira, Stella Amenta, Deniz Kanber, et al.
Journal of Medical Genetics
|
October 1, 1996
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome
B Horsthemke, A Maat-Kievit, E Sleegers, et al.
Journal of Medical Ethics
|
March 27, 2010
Dutch experience of monitoring active ending of life for newborns
Hilde M Buiting, Maartje A C Karelse, Hens A A Brouwers, et al.
American Journal of Human Genetics
|
February 11, 1999
Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation
T Ohta, K Buiting, H Kokkonen, et al.
Human Molecular Genetics
|
February 9, 1999
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities
Y Ji, M J Walkowicz, K Buiting, et al.
Acta Diabetologica
|
October 16, 2014
Cobalamin status and its relation with depression, cognition and neuropathy in patients with type 2 diabetes mellitus using metformin
Elke Biemans, Huberta E Hart, Guy E H M Rutten, et al.
American Journal of Human Genetics
|
December 1, 1999
A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?
K Buiting, B Dittrich, B Dworniczak, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 23, 1996
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations
S Saitoh, K Buiting, P K Rogan, et al.
Molecular Cytogenetics
|
October 3, 2014
Partial and complete trisomy 14 mosaicism: clinical follow-up, cytogenetic and molecular analysis
Consuelo Salas-Labadía, Esther Lieberman, Roberto Cruz-Alcívar, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
August 5, 2018
Spatial clustering and livestock exposure as risk factor for community-acquired Clostridium difficile infection
S M van Dorp, M P M Hensgens, O M Dekkers, et al.
Page
of 31