Search Results - McDonald-McGinn, Donna M.

Refine Results
  1. 1
    22q11.2 deletion syndrome: A tiny piece leading to a big picture

    22q11.2 deletion syndrome: A tiny piece leading to a big picture by McDonald-McGinn, Donna M.

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  2. 2
    Developmental Trajectories in 22q11.2 Deletion

    Developmental Trajectories in 22q11.2 Deletion by Swillen, Ann, McDonald-McGinn, Donna M.

    Published 2015
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  3. 3
    Aortic Root Dilation in Patients With 22q11.2 Deletion Syndrome

    Aortic Root Dilation in Patients With 22q11.2 Deletion Syndrome by John, Anitha S., McDonald-McGinn, Donna M., Zackai, Elaine H., Goldmuntz, Elizabeth

    Published 2009
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  4. 4
    Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome

    Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome by Crowley, Blaine, Ruffner, Melanie, McDonald McGinn, Donna M., Sullivan, Kathleen E.

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  5. 5
    Obituary of Dr. Angelo Di George

    Obituary of Dr. Angelo Di George by Tarani, Luigi, Digilio, Maria C, Dallapiccola, Bruno, Mc Donald-McGinn, Donna M, Marino, Bruno

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  6. 6
    CHARGE Syndrome and Chromosome 22q11.2 Deletion Syndrome: A Comparison of Immunologic and Non-Immunologic Phenotypic Features

    CHARGE Syndrome and Chromosome 22q11.2 Deletion Syndrome: A Comparison of Immunologic and Non-Immunologic Phenotypic Features by Jyonouchi, Soma, McDonald-McGinn, Donna M., Bale, Sherri, Zackai, Elaine H., Sullivan, Kathleen E.

    Published 2009
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  7. 7
    Molecular genetics of 22q11.2 deletion syndrome

    Molecular genetics of 22q11.2 deletion syndrome by Morrow, Bernice E., McDonald-McGinn, Donna M., Emanuel, Beverly S., Vermeesch, Joris R., Scambler, Peter J.

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  8. 8
    Pathways to understanding psychosis through rare – 22q11.2DS - and common variants

    Pathways to understanding psychosis through rare – 22q11.2DS - and common variants by Gur, Raquel E, Roalf, David R, Alexander-Bloch, Aaron, McDonald-McGinn, Donna M, Gur, Ruben C

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  9. 9
    Increased Prevalence of Immunoglobulin A Deficiency in Patients with the Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

    Increased Prevalence of Immunoglobulin A Deficiency in Patients with the Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome) by Smith, Christopher A., Driscoll, Deborah A., Emanuel, Beverly S., McDonald-McGinn, Donna M., Zackai, Elaine H., Sullivan, Kathleen E.

    Published 1998
    Get full text Get full text
    Text
    Save to List
    Saved in:
  10. 10
    Primary Amenorrhea and Absent Uterus in the 22q11.2 Deletion Syndrome

    Primary Amenorrhea and Absent Uterus in the 22q11.2 Deletion Syndrome by Sundaram, Usha T., McDonald-McGinn, Donna M., Huff, Dale, Emanuel, Beverly S., Zackai, Elaine H., Driscoll, Deborah A., Bodurtha, Joann

    Published 2007
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  11. 11
    Three Patients With Oculo-Auriculo-Vertebral Spectrum and Microdeletion 22q11.2

    Three Patients With Oculo-Auriculo-Vertebral Spectrum and Microdeletion 22q11.2 by Digilio, M. Cristina, McDonald-McGinn, Donna M., Heike, Carrie, Catania, Charles, Dallapiccola, Bruno, Marino, Bruno, Zackai, Elaine H.

    Published 2009
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  12. 12
    Speech-Language Disorders in 22q11.2 Deletion Syndrome: Best Practices for Diagnosis and Management

    Speech-Language Disorders in 22q11.2 Deletion Syndrome: Best Practices for Diagnosis and Management by Solot, Cynthia B., Sell, Debbie, Mayne, Anne, Baylis, Adriane L., Persson, Christina, Jackson, Oksana, McDonald-McGinn, Donna M.

    Published 2019
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  13. 13
    Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome

    Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome by Machado, Alexei M. C., Simon, Tony J., Nguyen, Vy, McDonald-McGinn, Donna M., Zackai, Elaine H., Gee, James C.

    Published 2006
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  14. 14
    Autism Spectrum Disorders and Symptoms in Children with Molecularly Confirmed 22q11.2 Deletion Syndrome

    Autism Spectrum Disorders and Symptoms in Children with Molecularly Confirmed 22q11.2 Deletion Syndrome by Fine, Sarah E., Weissman, Alison, Gerdes, Marsha, Pinto-Martin, Jennifer, Zackai, Elaine H., McDonald-McGinn, Donna M., Emanuel, Beverly S.

    Published 2005
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  15. 15
    Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome

    Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome by Hasten, Erica, McDonald-McGinn, Donna M, Crowley, Terrence B, Zackai, Elaine, Emanuel, Beverly S, Morrow, Bernice E, Racedo, Silvia E

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  16. 16
    A Prospective Study of Influenza Vaccination and a Comparison of Immunologic Parameters in Children and Adults with Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

    A Prospective Study of Influenza Vaccination and a Comparison of Immunologic Parameters in Children and Adults with Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocard... by Jawad, Abbas F., Prak, Eline Luning, Boyer, Jean, McDonald-McGinn, Donna M., Zackai, Elaine, McDonald, Kenyetta, Sullivan, Kathleen E.

    Published 2011
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  17. 17
    Anomalies of the Genitourinary Tract in Children with 22q11.2 Deletion Syndrome

    Anomalies of the Genitourinary Tract in Children with 22q11.2 Deletion Syndrome by Van Batavia, Jason P., Crowley, T. Blaine, Burrows, Evanette, Zackai, Elaine H., Sanna-Cherchi, Simone, McDonald-McGinn, Donna M., Kolon, Thomas F.

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  18. 18
    Association of hypocalcemia with congenital heart disease in 22q11.2 deletion syndrome

    Association of hypocalcemia with congenital heart disease in 22q11.2 deletion syndrome by Rayannavar, Arpana, Katz, Lorraine E. Levitt, Crowley, Terrence Blaine, Lessig, Megan, Grand, Katheryn, Goldmuntz, Elizabeth, Zackai, Elaine H., McDonald-McGinn, Donna M.

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  19. 19
    Mouse and Human CRKL Is Dosage Sensitive for Cardiac Outflow Tract Formation

    Mouse and Human CRKL Is Dosage Sensitive for Cardiac Outflow Tract Formation by Racedo, Silvia E., McDonald-McGinn, Donna M., Chung, Jonathan H., Goldmuntz, Elizabeth, Zackai, Elaine, Emanuel, Beverly S., Zhou, Bin, Funke, Birgit, Morrow, Bernice E.

    Published 2015
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  20. 20
    Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome

    Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome by Schindewolf, Erica, Khalek, Nahla, Johnson, Mark P., Gebb, Juliana, Coleman, Beverly, Crowley, Terrence Blaine, Zackai, Elaine H., McDonald-McGinn, Donna M., Moldenhauer, Julie S.

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:

Search Tools: