Search

Author/Creator Bailey, Alice

1. Cover Image, Volume 176A, Number 10, October 2018. Issue 10 (31st October 2018)

Authors:
Campbell, Ian M.; Sheppard, Sarah E.; Crowley, T. Blaine; McGinn, Daniel E.; Bailey, Alice; McGinn, Michael J.; Unolt, Marta; Homans, Jelle F.; Chen, Erin Y.; Salmons, Harold I.; Gaynor, J. William; Goldmuntz, Elizabeth; Jackson, Oksana A.; Katz, Lorraine E.; Mascarenhas, Maria R.; Deeney, Vincen...
Other Names:
McDonald‐McGinn Donna M. guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 10(2018)
Page Start:
i
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia. Issue 10 (31st October 2018)

Authors:
Campbell, Ian M.; Sheppard, Sarah E.; Crowley, T. Blaine; McGinn, Daniel E.; Bailey, Alice; McGinn, Michael J.; Unolt, Marta; Homans, Jelle F.; Chen, Erin Y.; Salmons, Harold I.; Gaynor, J. William; Goldmuntz, Elizabeth; Jackson, Oksana A.; Katz, Lorraine E.; Mascarenhas, Maria R.; Deeney, Vincen...
Other Names:
McDonald‐McGinn Donna M. guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 10(2018)
Page Start:
2058
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression. Issue 1 (16th September 2022)

Authors:
Campbell, Ian M.; Crowley, T. Blaine; Jobaliya, Chintan; Bailey, Alice; McGinn, Daniel E.; Gaiser, Kimberly; Bassett, Anne; Gur, Raquel E.; Morrow, Bernice; Emanuel, Beverly S.; Franco, Aime T.; French, Deborah; Zackai, Elaine H.; McDonald‐McGinn, Donna M.; Lambert, Michele P.
Journal:
Clinical genetics
Issue:
Volume 103:Issue 1(2023)
Page Start:
109
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS. Issue 2 (11th December 2012)

Authors:
McDonald-McGinn, Donna M; Fahiminiya, Somayyeh; Revil, Timothée; Nowakowska, Beata A; Suhl, Joshua; Bailey, Alice; Mlynarski, Elisabeth; Lynch, David R; Yan, Albert C; Bilaniuk, Larissa T; Sullivan, Kathleen E; Warren, Stephen T; Emanuel, Beverly S; Vermeesch, Joris R; Zackai, Elaine H; Jerome-Ma...
Journal:
Journal of medical genetics
Issue:
Volume 50:Issue 2(2013)
Page Start:
80
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Magnetic resonance angiography (MRA) in preoperative planning for patients with 22q11.2 deletion syndrome undergoing craniofacial and otorhinolaryngologic procedures. (November 2020)

Authors:
Kimia, Rotem; Elden, Lisa; Dailey, Julia; Kodavatiganti, Mallika; Crowley, T. Blaine; McGinn, Daniel E.; Bailey, Alice; Zackai, Elaine H.; McDonald-McGinn, Donna M.; Jackson, Oksana A.
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 138(2020:Nov.)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Cardiac evaluation of patients with 22q11.2 duplication syndrome. Issue 3 (27th December 2020)

Authors:
Butensky, Adam; de Rinaldis, Chiara Pandolfi; Patel, Shrey; Edman, Sharon; Bailey, Alice; McGinn, Daniel E.; Zackai, Elaine; Crowley, T. Blaine; McDonald‐McGinn, Donna M.; Min, Jungwon; Goldmuntz, Elizabeth
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 3(2021)
Page Start:
753
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗