The fetus & newly born infant : influences of the prenatal environment /

Por Stevenson, Roger E.
Publicado em 1973

The fetus and newly born infant influences of the prenatal environment /

Por Stevenson, Roger E.
Publicado em 1977

The fetus and newly born infant : Influences of the prenatal environment/.

Por Stevenson, Roger E.
Publicado em 1973

FETUS AND NEWLY BORN INFANT : INFLUENCES OF THE PRENATAL ENVIRONMENT.

Por STEVENSON, ROGER E.
Publicado em C1973

The MCT8 thyroid hormone transporter and Allan--Herndon--Dudley syndrome

Por Schwartz, Charles E., Stevenson, Roger E.
Publicado em 2007

Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery

Por Lubs, Herbert A., Stevenson, Roger E., Schwartz, Charles E.
Publicado em 2012

Malformations Among the X-Linked Intellectual Disability Syndromes

Por Stevenson, Roger E., Schwartz, Charles E., Rogers, R. Curtis
Publicado em 2013

The impact of spermine synthase (SMS) mutations on brain morphology

Por Kesler, Shelli R., Schwartz, Charles, Stevenson, Roger E., Reiss, Allan L.
Publicado em 2009

XLID Update 2017

Por Neri, Giovanni, Schwartz, Charles E., Lubs, Hebert A., Stevenson, Roger E.
Publicado no Am J Med Genet A (2018)

Seizures and X-linked intellectual disability

Por Stevenson, Roger E., Holden, Kenton R., Rogers, R. Curtis, Schwartz, Charles E.
Publicado em 2012

Long Term Maintenance of Neural Tube Defects Prevention in a High Prevalence State

Por Collins, Julianne S., Atkinson, Kristy K., Dean, Jane H., Best, Robert G., Stevenson, Roger E.
Publicado em 2011

AGTR2 in Brain Development and Function

Por Vervoort, Virginie S., Guzauskas, Greagory, Archie, John, Schwartz, Charles E., Stevenson, Roger E., Srivastava, Anand K.
Publicado em 2006

X chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation

Por Zhang, Lilei, Jie, Chunfa, Obie, Cassandra, Abidi, Fatima, Schwartz, Charles E., Stevenson, Roger E., Valle, David, Wang, Tao
Publicado em 2007

Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin–Lowry syndrome

Por Kesler, Shelli R., Simensen, Richard J., Voeller, Kytja, Abidi, Fatima, Stevenson, Roger E., Schwartz, Charles E., Reiss, Allan L.
Publicado em 2007

Duplication of OCRL and Adjacent Genes Associated with Autism but not Lowe Syndrome

Por Schroer, Richard J., Beaudet, Arthur L., Shinawi, Marwan, Sahoo, Trilochan, Patel, Ankita, Sun, Qin, Skinner, Cindy, Stevenson, Roger E.
Publicado em 2012

Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect, craniorachischisis

Por Robinson, Alexis, Escuin, Sarah, Doudney, Kit, Vekemans, Michel, Stevenson, Roger E, Greene, Nicholas DE, Copp, Andrew J, Stanier, Philip
Publicado no Hum Mutat (2011)

Phenotype and Genotype in Mucolipidoses II and III alpha/beta: A Study of 61 Probands

Por Cathey, Sara S., Leroy, Jules G., Wood, Tim, Eaves, Karisa, Simensen, Richard J., Kudo, Mariko, Stevenson, Roger E., Friez, Michael J.
Publicado em 2009

Craniofacioskeletal Syndrome: An X-Linked Dominant Disorder With Early Lethality in Males

Por Stevenson, Roger E., Brasington, Cam K., Skinner, Cindy, Simensen, Richard J., Spence, J. Edward, Kesler, Shelli, Reiss, Allan L., Schwartz, Charles E.
Publicado em 2007

A novel intermediate mucolipidosis II/IIIαβ caused by GNPTAB mutation in the cytosolic N-terminal domain

Por Leroy, Jules G, Sillence, David, Wood, Tim, Barnes, Jarrod, Lebel, Robert Roger, Friez, Michael J, Stevenson, Roger E, Steet, Richard, Cathey, Sara S
Publicado em 2014

Novel Truncating Mutations in the Polyglutamine Tract Binding Protein 1 Gene (PQBP1) Cause Renpenning Syndrome and X-Linked Mental Retardation in Another Family with Microcephaly

Por Lenski, Claus, Abidi, Fatima, Meindl, Alfons, Gibson, Alice, Platzer, Matthias, Frank Kooy, R., Lubs, Herbert A., Stevenson, Roger E., Ramser, Juliane, Schwartz, Charles E.
Publicado em 2004