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Journal of Medical Genetics
|
March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)
N J Lench, A F Markham, R F Mueller, et al.
Journal of the Neurological Sciences
|
March 1, 1992
The association of astrocytoma and pituitary adenoma in a patient with alcaptonuria
R Abs, M Van Vyve, P J Willems, et al.
Journal of Clinical Microbiology
|
March 27, 2015
What Is the Origin of Livestock-Associated Methicillin-Resistant Staphylococcus aureus Clonal Complex 398 Isolates from Humans without Livestock Contact? An Epidemiological and Genetic Analysis
W S N Lekkerkerk, W J B van Wamel, S V Snijders, et al.
Archives of Neurology
|
June 1, 1990
Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family
P J Willems, L Vits, R J Wanders, et al.
Journal of Medical Genetics
|
July 4, 2006
A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3
A S Brooks, P A Leegwater, G M Burzynski, et al.
Soft Matter
|
August 14, 2023
The dilatable membrane of oleosomes (lipid droplets) allows their <i>in vitro</i> resizing and triggered release of lipids
Eleni Ntone, Benjamin Rosenbaum, Simha Sridharan, et al.
Genomics
|
February 15, 1997
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q
P Coucke, G Van Camp, O Demirhan, et al.
The American Journal of Otology
|
September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locus
M Verstreken, F Declau, I Schatteman, et al.
The Journal of Antimicrobial Chemotherapy
|
December 7, 2010
Host range of enterococcal vanA plasmids among Gram-positive intestinal bacteria
Guido Werner, Ana R Freitas, Teresa M Coque, et al.
American Journal of Medical Genetics
|
September 13, 2000
Unexpected life-threatening complications in Kabuki syndrome
M M van Haelst, A S Brooks, J Hoogeboom, et al.
Page
of 45
Search research articles
Search
Showing results (381-390 of 446) with videos related to
Sort By:
Page
of 45
Journal of Medical Genetics
|
March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)
N J Lench, A F Markham, R F Mueller, et al.
Journal of the Neurological Sciences
|
March 1, 1992
The association of astrocytoma and pituitary adenoma in a patient with alcaptonuria
R Abs, M Van Vyve, P J Willems, et al.
Journal of Clinical Microbiology
|
March 27, 2015
What Is the Origin of Livestock-Associated Methicillin-Resistant Staphylococcus aureus Clonal Complex 398 Isolates from Humans without Livestock Contact? An Epidemiological and Genetic Analysis
W S N Lekkerkerk, W J B van Wamel, S V Snijders, et al.
Archives of Neurology
|
June 1, 1990
Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family
P J Willems, L Vits, R J Wanders, et al.
Journal of Medical Genetics
|
July 4, 2006
A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3
A S Brooks, P A Leegwater, G M Burzynski, et al.
Soft Matter
|
August 14, 2023
The dilatable membrane of oleosomes (lipid droplets) allows their <i>in vitro</i> resizing and triggered release of lipids
Eleni Ntone, Benjamin Rosenbaum, Simha Sridharan, et al.
Genomics
|
February 15, 1997
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q
P Coucke, G Van Camp, O Demirhan, et al.
The American Journal of Otology
|
September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locus
M Verstreken, F Declau, I Schatteman, et al.
The Journal of Antimicrobial Chemotherapy
|
December 7, 2010
Host range of enterococcal vanA plasmids among Gram-positive intestinal bacteria
Guido Werner, Ana R Freitas, Teresa M Coque, et al.
American Journal of Medical Genetics
|
September 13, 2000
Unexpected life-threatening complications in Kabuki syndrome
M M van Haelst, A S Brooks, J Hoogeboom, et al.
Page
of 45