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Genome
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November 18, 2000
Intercontinental karyotypic differentiation of Chironomus entis Shobanov, a Holarctic member of the C. plumosus group (Diptera, Chironomidae)
I I Kiknadze, M G Butler, V V Golygina, et al.
Histopathology
|
November 1, 1986
Cytokeratin and laminin immunostaining in the diagnosis of cutaneous neuro-endocrine (Merkel cell) tumours
P A Hall, A J d'Ardenne, M G Butler, et al.
Archives of Pathology & Laboratory Medicine
|
April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics Program
G W Dewald, A R Brothman, M G Butler, et al.
American Journal of Medical Genetics
|
March 1, 1996
Distinct 15q genotypes in Russell-Silver and ring 15 syndromes
P K Rogan, J R Seip, D J Driscoll, et al.
International Journal of Obesity (2005)
|
December 3, 2008
Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome
L M Holsen, J R Zarcone, R Chambers, et al.
International Journal of Obesity (2005)
|
May 5, 2010
Obese children show hyperactivation to food pictures in brain networks linked to motivation, reward and cognitive control
A S Bruce, L M Holsen, R J Chambers, et al.
The New England Journal of Medicine
|
June 11, 1992
The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis
M J Mascari, W Gottlieb, P K Rogan, et al.
Annals of the Rheumatic Diseases
|
October 1, 1992
Keratan sulphate in rheumatoid arthritis, osteoarthritis, and inflammatory diseases
T D Spector, L Woodward, G M Hall, et al.
Pediatric Obesity
|
December 28, 2018
Obestatin and adropin in Prader-Willi syndrome and nonsyndromic obesity: Associations with weight, BMI-z, and HOMA-IR
C E Orsso, A A Butler, M J Muehlbauer, et al.
Journal of Medical Genetics
|
April 5, 2005
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations
M G Butler, M J Dasouki, X-P Zhou, et al.
Page
of 17
Search research articles
Search
Showing results (151-160 of 165) with videos related to
Sort By:
Page
of 17
Genome
|
November 18, 2000
Intercontinental karyotypic differentiation of Chironomus entis Shobanov, a Holarctic member of the C. plumosus group (Diptera, Chironomidae)
I I Kiknadze, M G Butler, V V Golygina, et al.
Histopathology
|
November 1, 1986
Cytokeratin and laminin immunostaining in the diagnosis of cutaneous neuro-endocrine (Merkel cell) tumours
P A Hall, A J d'Ardenne, M G Butler, et al.
Archives of Pathology & Laboratory Medicine
|
April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics Program
G W Dewald, A R Brothman, M G Butler, et al.
American Journal of Medical Genetics
|
March 1, 1996
Distinct 15q genotypes in Russell-Silver and ring 15 syndromes
P K Rogan, J R Seip, D J Driscoll, et al.
International Journal of Obesity (2005)
|
December 3, 2008
Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome
L M Holsen, J R Zarcone, R Chambers, et al.
International Journal of Obesity (2005)
|
May 5, 2010
Obese children show hyperactivation to food pictures in brain networks linked to motivation, reward and cognitive control
A S Bruce, L M Holsen, R J Chambers, et al.
The New England Journal of Medicine
|
June 11, 1992
The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis
M J Mascari, W Gottlieb, P K Rogan, et al.
Annals of the Rheumatic Diseases
|
October 1, 1992
Keratan sulphate in rheumatoid arthritis, osteoarthritis, and inflammatory diseases
T D Spector, L Woodward, G M Hall, et al.
Pediatric Obesity
|
December 28, 2018
Obestatin and adropin in Prader-Willi syndrome and nonsyndromic obesity: Associations with weight, BMI-z, and HOMA-IR
C E Orsso, A A Butler, M J Muehlbauer, et al.
Journal of Medical Genetics
|
April 5, 2005
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations
M G Butler, M J Dasouki, X-P Zhou, et al.
Page
of 17