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American Journal of Medical Genetics
|
April 1, 1992
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?
G S Fisch, L R Shapiro, R Simensen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 15, 2013
Functional characterization of a heterozygous GLI2 missense mutation in patients with multiple pituitary hormone deficiency
G M C Flemming, J Klammt, G Ambler, et al.
Clinical Genetics
|
January 10, 2001
An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta
M S Peñaherrera, I J Barrett, C J Brown, et al.
Journal of Alzheimer'S Disease : JAD
|
July 16, 2014
Macular pigment, visual function, and macular disease among subjects with Alzheimer's disease: an exploratory study
John M Nolan, Ekaterina Loskutova, Alan N Howard, et al.
American Journal of Medical Genetics
|
June 1, 1987
ReCAP: the Registry of Cytogenetic Abnormalities and Phenylketonuria
J M Friedman, J P Smith, B N Lerner, et al.
The British Journal of Nutrition
|
October 13, 2000
Response of putative indices of copper status to copper supplementation in human subjects
C A Kehoe, E Turley, M P Bonham, et al.
Eye (London, England)
|
May 16, 2015
Sustained supplementation and monitored response with differing carotenoid formulations in early age-related macular degeneration
K O Akuffo, J M Nolan, A N Howard, et al.
American Journal of Medical Genetics
|
February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter study
G S Fisch, T Arinami, U Froster-Iskenius, et al.
Human Genetics
|
January 1, 1985
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
S L Sherman, P A Jacobs, N E Morton, et al.
American Journal of Medical Genetics
|
February 1, 1991
Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures
E C Jenkins, M S Krawczun, S L Stark-Houck, et al.
Page
of 42
Search research articles
Search
Showing results (381-390 of 411) with videos related to
Sort By:
Page
of 42
American Journal of Medical Genetics
|
April 1, 1992
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?
G S Fisch, L R Shapiro, R Simensen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 15, 2013
Functional characterization of a heterozygous GLI2 missense mutation in patients with multiple pituitary hormone deficiency
G M C Flemming, J Klammt, G Ambler, et al.
Clinical Genetics
|
January 10, 2001
An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta
M S Peñaherrera, I J Barrett, C J Brown, et al.
Journal of Alzheimer'S Disease : JAD
|
July 16, 2014
Macular pigment, visual function, and macular disease among subjects with Alzheimer's disease: an exploratory study
John M Nolan, Ekaterina Loskutova, Alan N Howard, et al.
American Journal of Medical Genetics
|
June 1, 1987
ReCAP: the Registry of Cytogenetic Abnormalities and Phenylketonuria
J M Friedman, J P Smith, B N Lerner, et al.
The British Journal of Nutrition
|
October 13, 2000
Response of putative indices of copper status to copper supplementation in human subjects
C A Kehoe, E Turley, M P Bonham, et al.
Eye (London, England)
|
May 16, 2015
Sustained supplementation and monitored response with differing carotenoid formulations in early age-related macular degeneration
K O Akuffo, J M Nolan, A N Howard, et al.
American Journal of Medical Genetics
|
February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter study
G S Fisch, T Arinami, U Froster-Iskenius, et al.
Human Genetics
|
January 1, 1985
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
S L Sherman, P A Jacobs, N E Morton, et al.
American Journal of Medical Genetics
|
February 1, 1991
Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures
E C Jenkins, M S Krawczun, S L Stark-Houck, et al.
Page
of 42