खोज परिणाम - Stevenson, Roger
- प्रदर्शित 1 - 20 परिणाम 78
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XLID Update 2017 द्वारा Neri, Giovanni, Schwartz, Charles E., Lubs, Hebert A., Stevenson, Roger E.
प्रकाशित 2018मूलपाठ -
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Affected Kindred Analysis of Human X Chromosome Exomes to Identify Novel X-Linked Intellectual Disability Genes द्वारा Niranjan, Tejasvi S., Skinner, Cindy, May, Melanie, Turner, Tychele, Rose, Rebecca, Stevenson, Roger, Schwartz, Charles E., Wang, Tao
प्रकाशित 2015मूलपाठ -
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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 2007मूलपाठ -
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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 2007मूलपाठ -
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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 2012मूलपाठ -
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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
प्रकाशित 2011मूलपाठ -
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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 2009मूलपाठ -
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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 2007मूलपाठ -
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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 2014मूलपाठ -
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Abnormalities in the genes that encode Large Amino Acid Transporters increase the risk of Autism Spectrum Disorder द्वारा Cascio, Lauren, Chen, Chin‐Fu, Pauly, Rini, Srikanth, Sujata, Jones, Kelly, Skinner, Cindy D., Stevenson, Roger E., Schwartz, Charles E., Boccuto, Luigi
प्रकाशित 2019मूलपाठ -
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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 द्वारा Lenski, Claus, Abidi, Fatima, Meindl, Alfons, Gibson, Alice, Platzer, Matthias, Frank Kooy, R., Lubs, Herbert A., Stevenson, Roger E., Ramser, Juliane, Schwartz, Charles E.
प्रकाशित 2004मूलपाठ