Author Search Results

1

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

Published 1972

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Vertigo by Graham, John M

Published 1985

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

Published 1980

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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 by Graham, John M.

Published 2011

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

Published 2002

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

Published 2006

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

Published 2013

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

Published 2009

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

Published 2012

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

Published 2013

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11

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

Published 2003

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

Published 2012

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

Published 2009

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14

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

Published 2012

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

Published 2010

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

Published 2012

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

Published 2015

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

Published 2021

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19

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

Published 2009

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

Published 2010

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Search Results - Graham, John M.

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

Vertigo by Graham, John M

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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