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Annals of Neurology
|
February 9, 2000
Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study
K M Flanigan, L Kerr, M B Bromberg, et al.
American Journal of Human Genetics
|
February 11, 1999
Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q
M R Hobbs, A R Pole, G N Pidwirny, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
Sequential neuromotor examination of children with intrauterine drug exposure
H M Belcher, B K Shapiro, M Leppert, et al.
Nano Letters
|
March 21, 2018
Giant Mechano-Optoelectronic Effect in an Atomically Thin Semiconductor
Wei Wu, Jin Wang, Peter Ercius, et al.
Human Molecular Genetics
|
June 1, 1992
Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22
M R Hoehe, R Plaetke, B Otterud, et al.
Genomics
|
February 10, 1995
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1
C A Klanke, Y R Su, D F Callen, et al.
Nature
|
April 5, 1990
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3
L M Brzustowicz, T Lehner, L H Castilla, et al.
Developmental Medicine and Child Neurology
|
June 4, 1999
Sequential neuromotor examination in children with intrauterine cocaine/polydrug exposure
H M Belcher, B K Shapiro, M Leppert, et al.
Brain Pathology (Zurich, Switzerland)
|
October 1, 1993
Searching for human epilepsy genes: a progress report
M Leppert, W M McMahon, T G Quattlebaum, et al.
Investigative Ophthalmology & Visual Science
|
December 1, 2001
Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene
P S Bernstein, J Tammur, N Singh, et al.
Page
of 32
Search research articles
Search
Showing results (281-290 of 315) with videos related to
Sort By:
Page
of 32
Annals of Neurology
|
February 9, 2000
Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study
K M Flanigan, L Kerr, M B Bromberg, et al.
American Journal of Human Genetics
|
February 11, 1999
Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q
M R Hobbs, A R Pole, G N Pidwirny, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
Sequential neuromotor examination of children with intrauterine drug exposure
H M Belcher, B K Shapiro, M Leppert, et al.
Nano Letters
|
March 21, 2018
Giant Mechano-Optoelectronic Effect in an Atomically Thin Semiconductor
Wei Wu, Jin Wang, Peter Ercius, et al.
Human Molecular Genetics
|
June 1, 1992
Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22
M R Hoehe, R Plaetke, B Otterud, et al.
Genomics
|
February 10, 1995
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1
C A Klanke, Y R Su, D F Callen, et al.
Nature
|
April 5, 1990
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3
L M Brzustowicz, T Lehner, L H Castilla, et al.
Developmental Medicine and Child Neurology
|
June 4, 1999
Sequential neuromotor examination in children with intrauterine cocaine/polydrug exposure
H M Belcher, B K Shapiro, M Leppert, et al.
Brain Pathology (Zurich, Switzerland)
|
October 1, 1993
Searching for human epilepsy genes: a progress report
M Leppert, W M McMahon, T G Quattlebaum, et al.
Investigative Ophthalmology & Visual Science
|
December 1, 2001
Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene
P S Bernstein, J Tammur, N Singh, et al.
Page
of 32