Progress toward integrating care for seniors in Canada: “We have to skate toward where the puck is going to be, not to where it has been.”

Por MacAdam, Margaret
Publicado em 2011

PRISMA: Program of Research to Integrate the Services for the Maintenance of Autonomy. A system-level integration model in Quebec

Por MacAdam, Margaret
Publicado no Int J Integr Care (2015)

EVALUATION AND DIAGNOSIS OF THE DYSMORPHIC INFANT

Por Jones, Kelly L., Adam, Margaret P.
Publicado no Clin Perinatol (2015)

Evaluation of a Cervical Cancer Screening Program Based on HPV Testing and LLETZ Excision in a Low Resource Setting

Por McAdam, Margaret, Sakita, Jerol, Tarivonda, Len, Pang, James, Frazer, Ian H.
Publicado em 2010

Detailed characterization of and clinical correlations in ten patients with distal deletions of chromosome 9p

Por Hauge, Xueya, Raca, Gordana, Cooper, Sara, May, Kristin, Spiro, Rhonda, Adam, Margaret, Martin, Lese
Publicado em 2008

A Homozygous B3GAT3 Mutation Causes a Severe Syndrome with Multiple Fractures, Extending the Number of Linkeropathy Syndromes

Por Jones, Kelly L., Schwarze, Ulrike, Adam, Margaret P., Byers, Peter H., Mefford, Heather C.
Publicado no Am J Med Genet A (2015)

Clinical Utility of Array Comparative Genomic Hybridization: Uncovering Tumor Susceptibility in Individuals with Developmental Delay

Por Adam, Margaret P., Justice, April N., Schelley, Susan, Kwan, Andrea, Hudgins, Louanne, Martin, Christa L.
Publicado em 2009

A descriptive framework for new hospital roles in geriatric care

Por Capitman, John A., Prottas, Jeffrey, MacAdam, Margaret, Leutz, Walter, Westwater, Don, Yee, Donna L.
Publicado em 1988

Novel pregnancy-triggered episodes of CAPOS syndrome

Por Chang, Irene J., Adam, Margaret P., Jayadev, Suman, Bird, Thomas D., Natarajan, Niranjana, Glass, Ian A.
Publicado no Am J Med Genet A (2017)

Allelic Dropout Can Cause False-Positive Results for Prader-Willi and Angelman Syndrome Testing

Por Hussain Askree, Syed, Hjelm, Lawrence N., Ali Pervaiz, Muhammad, Adam, Margaret, Bean, Lora J.H., Hedge, Madhuri, Coffee, Bradford
Publicado em 2011

Description of A New Oncogenic Mechanism for Atypical Teratoid Rhabdoid Tumors in Patients with Ring Chromosome 22

Por Byers, Heather M., Adam, Margaret P., LaCroix, Amy, Leary, Sarah E.S., Cole, Bonnie, Dobyns, William B., Mefford, Heather C.
Publicado no Am J Med Genet A (2016)

Segmental duplications mediate novel, clinically relevant chromosome rearrangements

Por Rudd, M. Katharine, Keene, Julia, Bunke, Brian, Kaminsky, Erin B., Adam, Margaret P., Mulle, Jennifer G., Ledbetter, David H., Martin, Christa L.
Publicado em 2009

Persistent figure-8 and side-to-side head shaking is a marker for rhombencephalosynapsis

Por Tully, Hannah M, Dempsey, Jennifer C, Ishak, Gisele E, Adam, Margaret P, Mink, Jonathan W, Dobyns, William B, Gospe, Sidney M, Weiss, Avery, Phillips, James O, Doherty, Dan
Publicado no Mov Disord (2013)

Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity

Por Ishak, Gisele E., Dempsey, Jennifer C., Shaw, Dennis W. W., Tully, Hannah, Adam, Margaret P., Sanchez-Lara, Pedro A., Glass, Ian, Rue, Tessa C., Millen, Kathleen J., Dobyns, William B., Doherty, Dan
Publicado em 2012

Sclerocornea Associated With the Chromosome 22q11.2 Deletion Syndrome

Por Binenbaum, Gil, McDonald-McGinn, Donna M., Zackai, Elaine H., Walker, B. Michael, Coleman, Karlene, Mach, Amy M., Adam, Margaret, Manning, Melanie, Alcorn, Deborah M., Zabel, Carrie, Anderson, Dennis R., Forbes, Brian J.
Publicado em 2008

Prevalence and Characteristics of Fetal Alcohol Spectrum Disorders

Por May, Philip A., Baete, Amy, Russo, Jaymi, Elliott, Amy J., Blankenship, Jason, Kalberg, Wendy O., Buckley, David, Brooks, Marita, Hasken, Julie, Abdul-Rahman, Omar, Adam, Margaret P., Robinson, Luther K., Manning, Melanie, Hoyme, H. Eugene
Publicado em 2014

A South African Mixed Race Lip/Philtrum Guide for Diagnosis of Fetal Alcohol Spectrum Disorders

Por Hoyme, H. Eugene, Hoyme, Derek B., Elliott, Amy J., Blankenship, Jason, Kalberg, Wendy O., Buckley, David, Abdul-Rahman, Omar, Adam, Margaret P., Robinson, Luther K., Manning, Melanie, Bezuidenhout, Heidre, Jones, Kenneth L., May, Philip A.
Publicado no Am J Med Genet A (2015)

Beyond Gómez-López-Hernández Syndrome: Recurring Phenotypic Themes in Rhombencephalosynapsis

Por Tully, Hannah M, Dempsey, Jennifer C, Ishak, Gisele E, Adam, Margaret P, Curry, Cynthia JR, Sanchez-Lara, Pedro, Hunter, Alasdair, Gripp, Karen W, Allanson, Judith, Cunniff, Christopher, Glass, Ian, Millen, Kathleen J, Doherty, Daniel, Dobyns, William B
Publicado em 2012

A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes

Por Shlien, Adam, Baskin, Berivan, Achatz, Maria Isabel W., Stavropoulos, Dimitrios J., Nichols, Kim E., Hudgins, Louanne, Morel, Chantal F., Adam, Margaret P., Zhukova, Nataliya, Rotin, Lianne, Novokmet, Ana, Druker, Harriet, Shago, Mary, Ray, Peter N., Hainaut, Pierre, Malkin, David
Publicado em 2010

Unexpected Ethical Dilemmas in Sex Assignment in 46,XY DSD due to 5-alpha Reductase Type 2 Deficiency

Por Byers, Heather M., Mohnach, Lauren H., Fechner, Patricia Y., Chen, Ming, Thomas, Inas H., Ramsdell, Linda A., Shnorhavorian, Margaret, McCauley, Elizabeth, Amies Oelschlager, Anne-Marie E., Park, John M., Sandberg, David E., Adam, Margaret P., Keegan, Catherine E.
Publicado no Am J Med Genet C Semin Med Genet (2017)