C E Schwartz

New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder–Robinson X-linked recessive mental retardation syndrome

C. Schwartz, M. Passos-Bueno, A. Pegg, 2008, Journal of Medical Genetics.

Non‐syndromic X‐linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene

R R Lebel, Rebekah K. Stevenson, H A Lubs, 2002, Clinical genetics.

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects.

C Y Ou, M J Khoury, M. Khoury, 1996, American journal of medical genetics.

Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system

M. Bellgrove, C. Schwartz, C. Claudianos, 2014, Molecular Psychiatry.

A missense mutation, p.V132G, in the X‐linked spermine synthase gene (SMS) causes Snyder–Robinson syndrome

J. Śanchez-Corona, J. García-Ortiz, D E McCloskey, 2009, American journal of medical genetics. Part A.