C. Brewer

Effects of Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) participation on household food availability

C. Brewer, 2014 .

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

G. J. Swaminathan, N. Carter, M. Hurles, 2019, American journal of human genetics.

Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing

S. Ellard, B. Vaidya, A. Hattersley, 2005, Clinical endocrinology.

X‐Linked Hydrocephalus Masquerading as Spina Bifida and Destructive Porencephaly in Successive Generations in One Family

J. Tolmie, J. Stephenson, C. Brewer, 1996, Developmental medicine and child neurology.

diagnosis of Williams syndrome . Clinical and molecular cytogenetic ( FISH )

J. Tolmie, N. Morrison, C. Brewer, 2006 .

Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome.

J. Tolmie, N. Morrison, C. Brewer, 1996, Archives of disease in childhood.

X‐Linked Hydrocephalus Masquerading as Spina Bifida and Destructive Porencephaly in Successive Generations in One Family

J. Stephenson, C. Brewer, B. Fredericks, 1996, Developmental medicine and child neurology.