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Genome Medicine
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June 13, 2022
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome
Margot A Cousin, Emma L Veale, Nikita R Dsouza, et al.
European Journal of Human Genetics : EJHG
|
October 25, 2024
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations
Angela Peron, Felice D'Arco, Kimberly A Aldinger, et al.
Brain : a Journal of Neurology
|
September 4, 2021
Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
Manuela Wiessner, Reza Maroofian, Meng-Yuan Ni, et al.
Brain : a Journal of Neurology
|
May 10, 2021
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
Manuela Wiessner, Reza Maroofian, Meng-Yuan Ni, et al.
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of 3
Search research articles
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Showing results (21-30 of 24) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 24 results.
Genome Medicine
|
June 13, 2022
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome
Margot A Cousin, Emma L Veale, Nikita R Dsouza, et al.
European Journal of Human Genetics : EJHG
|
October 25, 2024
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations
Angela Peron, Felice D'Arco, Kimberly A Aldinger, et al.
Brain : a Journal of Neurology
|
September 4, 2021
Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
Manuela Wiessner, Reza Maroofian, Meng-Yuan Ni, et al.
Brain : a Journal of Neurology
|
May 10, 2021
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
Manuela Wiessner, Reza Maroofian, Meng-Yuan Ni, et al.
Page
of 3