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L T Middleton

Showing results (21-30 of 38) with videos related to

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Psychological Medicine|February 15, 2008
Family history of depression is associated with younger age of onset in patients with recurrent depressionF Tozzi, I Prokopenko, J D Perry, et al.
The Journal of Prevention of Alzheimer'S Disease|October 1, 2024
Lower Incidence of Dementia Following Cancer Diagnoses: Evidence from a Large Cohort and Mendelian Randomization StudyD T Bassil, B Zheng, B Su, et al.
Human Molecular Genetics|April 1, 1997
Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneityK Christodoulou, M Tsingis, F Deymeer, et al.
The Journal of General Physiology|August 30, 2000
Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndromeH L Wang, K Ohno, M Milone, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversityL T Middleton, K Christodoulou, F Deymeer, et al.
Genomics|August 1, 1993
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneityK Ben Othmane, L T Middleton, L J Loprest, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Distal hereditary motor neuronopathy of the Jerash typeL T Middleton, K Christodoulou, A Mubaidin, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Distal Hereditary Motor Neuronopathy of the Jerash TypeL T Middleton, K Christodoulou, A Mubaidin, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Distal hereditary motor neuronopathy of the Jerash typeL T Middleton, K Christodoulou, A Mubaidin, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Distal Hereditary Motor Neuronopathy of the Jerash TypeL T Middleton, K Christodoulou, A Mubaidin, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Psychological Medicine|February 15, 2008
Family history of depression is associated with younger age of onset in patients with recurrent depressionF Tozzi, I Prokopenko, J D Perry, et al.
The Journal of Prevention of Alzheimer'S Disease|October 1, 2024
Lower Incidence of Dementia Following Cancer Diagnoses: Evidence from a Large Cohort and Mendelian Randomization StudyD T Bassil, B Zheng, B Su, et al.
Human Molecular Genetics|April 1, 1997
Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneityK Christodoulou, M Tsingis, F Deymeer, et al.
The Journal of General Physiology|August 30, 2000
Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndromeH L Wang, K Ohno, M Milone, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversityL T Middleton, K Christodoulou, F Deymeer, et al.
Genomics|August 1, 1993
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneityK Ben Othmane, L T Middleton, L J Loprest, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Distal hereditary motor neuronopathy of the Jerash typeL T Middleton, K Christodoulou, A Mubaidin, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Distal Hereditary Motor Neuronopathy of the Jerash TypeL T Middleton, K Christodoulou, A Mubaidin, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Distal hereditary motor neuronopathy of the Jerash typeL T Middleton, K Christodoulou, A Mubaidin, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Distal Hereditary Motor Neuronopathy of the Jerash TypeL T Middleton, K Christodoulou, A Mubaidin, et al.
Pageof 4