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American Journal of Medical Genetics|July 12, 1996
Molecular fragile X screening in normal populationsW C Spence, S H Black, L Fallon, et al.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 deficiencyG 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 placentaM 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 studyJohn M Nolan, Ekaterina Loskutova, Alan N Howard, et al.American Journal of Medical Genetics|June 1, 1987
ReCAP: the Registry of Cytogenetic Abnormalities and PhenylketonuriaJ 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 subjectsC 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 degenerationK 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 studyG 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 malesS L Sherman, P A Jacobs, N E Morton, et al.Pageof 23