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Hepatology (Baltimore, Md.)
|
December 1, 1994
FK 506 renal toxicity and lack of detectable cytochrome P-450 3A in the liver graft of a patient undergoing liver transplantation
A Lemoine, D Azoulay, A Dennison, et al.
Neurology
|
April 25, 2008
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome
J Nectoux, N Bahi-Buisson, I Guellec, et al.
Vascular Pharmacology
|
September 27, 2005
Reduced exhaled NO is related to impaired nasal potential difference in patients with cystic fibrosis
J Texereau, I Fajac, D Hubert, et al.
Annales De Genetique
|
May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation
P Billuart, J Chelly, A Carrié, et al.
Human Mutation
|
August 29, 2001
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy
T Bienvenu, I Souville, K Poirier, et al.
Human Reproduction (Oxford, England)
|
January 15, 2005
Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study
I E Aknin-Seifer, R L Touraine, H Lejeune, et al.
American Journal of Human Genetics
|
April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28
V des Portes, P Billuart, A Carrié, et al.
Clinical Genetics
|
April 30, 2017
The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function
C T Gordon, A Tessier, Z Demir, et al.
American Journal of Medical Genetics
|
October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24
V des Portes, N Soufir, A Carrié, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
April 25, 2020
Penetrance is a critical parameter for assessing the disease liability of CFTR variants
A Boussaroque, M-P Audrézet, C Raynal, et al.
Page
of 10
Search research articles
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Showing results (51-60 of 92) with videos related to
Sort By:
Page
of 10
Hepatology (Baltimore, Md.)
|
December 1, 1994
FK 506 renal toxicity and lack of detectable cytochrome P-450 3A in the liver graft of a patient undergoing liver transplantation
A Lemoine, D Azoulay, A Dennison, et al.
Neurology
|
April 25, 2008
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome
J Nectoux, N Bahi-Buisson, I Guellec, et al.
Vascular Pharmacology
|
September 27, 2005
Reduced exhaled NO is related to impaired nasal potential difference in patients with cystic fibrosis
J Texereau, I Fajac, D Hubert, et al.
Annales De Genetique
|
May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation
P Billuart, J Chelly, A Carrié, et al.
Human Mutation
|
August 29, 2001
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy
T Bienvenu, I Souville, K Poirier, et al.
Human Reproduction (Oxford, England)
|
January 15, 2005
Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study
I E Aknin-Seifer, R L Touraine, H Lejeune, et al.
American Journal of Human Genetics
|
April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28
V des Portes, P Billuart, A Carrié, et al.
Clinical Genetics
|
April 30, 2017
The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function
C T Gordon, A Tessier, Z Demir, et al.
American Journal of Medical Genetics
|
October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24
V des Portes, N Soufir, A Carrié, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
April 25, 2020
Penetrance is a critical parameter for assessing the disease liability of CFTR variants
A Boussaroque, M-P Audrézet, C Raynal, et al.
Page
of 10