Sökresultat - Graham, John M.

Isolation and characterization of membranes from normal and transformed tissue-culture cells av Graham, John M.

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Vertigo av Graham, John M

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Auditory Investigation: the Scientific and Technological Basis av Graham, John M

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GLUT1 deficiency syndrome as a cause of encephalopathy that includes cognitive disability, treatment-resistant infantile epilepsy and a complex movement disorder av Graham, John M.

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OptiPrep Density Gradient Solutions for Nonmammalian Organelles av Graham, John M.

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Klinefelter syndrome and other sex chromosomal aneuploidies av Visootsak, Jeannie, Graham, John M

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Expanding our knowledge of conditions associated with the ASXL gene family av Russell, Bianca, Graham, John M

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Social Function in Multiple X and Y Chromosome Disorders: XXY, XYY, XXYY, XXXY av Visootsak, Jeannie, Graham, John M.

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Ichthyotic Skin Disorders in the Neonate av Rimoin, Lauren, Graham, John M.

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MED12 Related Disorders av Graham, John M., Schwartz, Charles E.

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Iodixanol Density Gradient Preparation in University of Wisconsin Solution for Porcine Islet Purification av Van der Burg, Michael P.M., Graham, John M.

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Clinical review of genetic epileptic encephalopathies av Noh, Grace J., Asher, Y. Jane Tavyev, Graham, John M.

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A 785 kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis av Pariani, Mitchel J., Spencer, Andrew, Graham, John M., Rimoin, David L.

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Extrinsic Factors Influencing Fetal Deformations and Intrauterine Growth Restriction av Moh, Wendy, Graham, John M., Wadhawan, Isha, Sanchez-Lara, Pedro A.

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Behavioral Features in Young Adults with FG Syndrome (Opitz-Kaveggia Syndrome) av Graham, John M, Clark, Robin D, Moeschler, John B, Rogers, R. Curtis

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Growth retardation, intellectual disability, facial anomalies, cataract, thoracic hypoplasia and skeletal abnormalities: a novel phenotype av Shah, Hitesh, Bens, Susanne, Caliebe, Almuth, Graham, John M., Girisha, Katta Mohan

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Mutation in the sixth immunoglobulin domain of L1CAM is associated with migrational brain anomalies av Shieh, Christine, Moser, Franklin, Graham, John M., Watiker, Valerie, Pierson, Tyler Mark

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Spontaneous intracranial hypotension secondary to congenital spinal dural ectasia and genetic mosaicism for tetrasomy 10p: illustrative case av Nisson, Peyton L., Schreck, Rhona, Graham, John M., Maya, Marcel M., Schievink, Wouter I.

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Genomic Duplication of PTPN11 is an Uncommon Cause of Noonan Syndrome av Graham, John M., Kramer, Nancy, Bejjani, Bassem A., Thiel, Christian T., Carta, Claudio, Neri, Giovanni, Tartaglia, Marco, Zenker, Martin

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Severe Cleidocranial dysplasia and Hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2 av El-Gharbawy, Areeg H., Peeden, Joseph N., Lachman, Ralph S., Graham, John M., Moore, Stephen R., Rimoin, David L.

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