Developmental Trajectories in 22q11.2 Deletion

Por Swillen, Ann, McDonald-McGinn, Donna M.
Publicado no Am J Med Genet C Semin Med Genet (2015)

CD4(+) CD25(+) T-Cell Production in Healthy Humans and in Patients with Thymic Hypoplasia

Por Sullivan, Kathleen E., McDonald-McGinn, Donna, Zackai, Elaine H.
Publicado em 2002

Modification by prostaglandin E(2) (PGE(2)) of the response of guinea-pig isolated vasa deferentia and atria to adrenergic stimuli

Por Bhagat, B., Dhalla, N. S., Ginn, Donna, La Montagne, A. E., Montier, A. D.
Publicado em 1972

Aortic Root Dilation in Patients With 22q11.2 Deletion Syndrome

Por John, Anitha S., McDonald-McGinn, Donna M., Zackai, Elaine H., Goldmuntz, Elizabeth
Publicado em 2009

VISUOSPATIAL AND NUMERICAL COGNITIVE DEFICITS IN CHILDREN WITH CHROMOSOME 22Q11.2 DELETION SYNDROME

Por Simon, Tony J., Bearden, Carrie E., Mc-Ginn, Donna McDonald, Zackai, Elaine
Publicado no Cortex (2005)

Obituary of Dr. Angelo Di George

Por Mc Donald-McGinn Donna M, Dallapiccola Bruno, Digilio Maria C, Tarani Luigi, Marino Bruno
Publicado em 2010-03-01

Obituary of Dr. Angelo Di George

Por Tarani, Luigi, Digilio, Maria C, Dallapiccola, Bruno, Mc Donald-McGinn, Donna M, Marino, Bruno
Publicado em 2010

CHARGE Syndrome and Chromosome 22q11.2 Deletion Syndrome: A Comparison of Immunologic and Non-Immunologic Phenotypic Features

Por Jyonouchi, Soma, McDonald-McGinn, Donna M., Bale, Sherri, Zackai, Elaine H., Sullivan, Kathleen E.
Publicado em 2009

Molecular genetics of 22q11.2 deletion syndrome

Por Morrow, Bernice E., McDonald-McGinn, Donna M., Emanuel, Beverly S., Vermeesch, Joris R., Scambler, Peter J.
Publicado no Am J Med Genet A (2018)

Longitudinal Analysis of Lymphocyte Function and Numbers in the First Year of Life in Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

Por Sullivan, Kathleen E., McDonald-McGinn, Donna, Driscoll, Deborah A., Emanuel, Beverly S., Zackai, Elaine H., Jawad, Abbas F.
Publicado em 1999

Evaluation of Potential Modifiers of the Cardiac Phenotype in the 22q11.2 Deletion Syndrome

Por Goldmuntz, Elizabeth, Driscoll, Deborah A., Emanuel, Beverly S., McDonald-McGinn, Donna, Mei, Minghua, Zackai, Elaine, Mitchell, Laura E.
Publicado em 2009

Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series

Por Butcher, Nancy J., Boot, Erik, Lang, Anthony E., Andrade, Danielle, Vorstman, Jacob, McDonald-McGinn, Donna, Bassett, Anne S.
Publicado no Am J Med Genet A (2018)

Increased Prevalence of Immunoglobulin A Deficiency in Patients with the Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

Por Smith, Christopher A., Driscoll, Deborah A., Emanuel, Beverly S., McDonald-McGinn, Donna M., Zackai, Elaine H., Sullivan, Kathleen E.
Publicado em 1998

Primary Amenorrhea and Absent Uterus in the 22q11.2 Deletion Syndrome

Por Sundaram, Usha T., McDonald-McGinn, Donna M., Huff, Dale, Emanuel, Beverly S., Zackai, Elaine H., Driscoll, Deborah A., Bodurtha, Joann
Publicado em 2007

Three Patients With Oculo-Auriculo-Vertebral Spectrum and Microdeletion 22q11.2

Por Digilio, M. Cristina, McDonald-McGinn, Donna M., Heike, Carrie, Catania, Charles, Dallapiccola, Bruno, Marino, Bruno, Zackai, Elaine H.
Publicado em 2009

Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome

Por Machado, Alexei M. C., Simon, Tony J., Nguyen, Vy, McDonald-McGinn, Donna M., Zackai, Elaine H., Gee, James C.
Publicado em 2006

Autism Spectrum Disorders and Symptoms in Children with Molecularly Confirmed 22q11.2 Deletion Syndrome

Por Fine, Sarah E., Weissman, Alison, Gerdes, Marsha, Pinto-Martin, Jennifer, Zackai, Elaine H., McDonald-McGinn, Donna M., Emanuel, Beverly S.
Publicado em 2005

Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome

Por Hasten, Erica, McDonald-McGinn, Donna M, Crowley, Terrence B, Zackai, Elaine, Emanuel, Beverly S, Morrow, Bernice E, Racedo, Silvia E
Publicado no Hum Mol Genet (2018)

Mouse and Human CRKL Is Dosage Sensitive for Cardiac Outflow Tract Formation

Por Racedo, Silvia E., McDonald-McGinn, Donna M., Chung, Jonathan H., Goldmuntz, Elizabeth, Zackai, Elaine, Emanuel, Beverly S., Zhou, Bin, Funke, Birgit, Morrow, Bernice E.
Publicado no Am J Hum Genet (2015)

The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder

Por Wenger, Tara L., Kao, Charlly, McDonald-McGinn, Donna M., Zackai, Elaine H., Bailey, Alice, Schultz, Robert T., Morrow, Bernice E., Emanuel, Beverly S., Hakonarson, Hakon
Publicado no Sci Rep (2016)