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

द्वारा STEVENSON, ROGER E.
प्रकाशित C1973

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

द्वारा Stevenson, Roger E.
प्रकाशित 1973.

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

द्वारा Stevenson, Roger E.
प्रकाशित 1977.

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

द्वारा Stevenson, Roger E.
प्रकाशित 1973.

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

द्वारा Schwartz, Charles E., Stevenson, Roger E.
प्रकाशित 2007

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

द्वारा Lubs, Herbert A., Stevenson, Roger E., Schwartz, Charles E.
प्रकाशित 2012

Malformations Among the X-Linked Intellectual Disability Syndromes

द्वारा Stevenson, Roger E., Schwartz, Charles E., Rogers, R. Curtis
प्रकाशित 2013

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

द्वारा Kesler, Shelli R., Schwartz, Charles, Stevenson, Roger E., Reiss, Allan L.
प्रकाशित 2009

XLID Update 2017

द्वारा Neri, Giovanni, Schwartz, Charles E., Lubs, Hebert A., Stevenson, Roger E.
में प्रकाशित Am J Med Genet A (2018)

Seizures and X-linked intellectual disability

द्वारा Stevenson, Roger E., Holden, Kenton R., Rogers, R. Curtis, Schwartz, Charles E.
प्रकाशित 2012

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

द्वारा Collins, Julianne S., Atkinson, Kristy K., Dean, Jane H., Best, Robert G., Stevenson, Roger E.
प्रकाशित 2011

AGTR2 in Brain Development and Function

द्वारा Vervoort, Virginie S., Guzauskas, Greagory, Archie, John, Schwartz, Charles E., Stevenson, Roger E., Srivastava, Anand K.
प्रकाशित 2006

UBE2A-Related X-linked Intellectual Disability

द्वारा Stevenson, Roger E., Chudley, Albert E., Srivastava, Anand K., Rodriguez, Jayson, Friez, Michael J., Schwartz, Charles E.
में प्रकाशित Clin Dysmorphol (2019)

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

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

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

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

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

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

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

द्वारा Robinson, Alexis, Escuin, Sarah, Doudney, Kit, Vekemans, Michel, Stevenson, Roger E, Greene, Nicholas DE, Copp, Andrew J, Stanier, Philip
में प्रकाशित Hum Mutat (2011)

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

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

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

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

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

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