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/vufind/Search/Results?lookfor=%22McDonald-McGinn%2C+Donna%C2%A0M.%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22McDonald-McGinn%2C+Donna%C2%A0M.%22&type=Person&sort=year
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PubPharm (350)
1
Platelet findings in 22q11.2 Deletion Syndrome correlate with disease manifestations but do not correlate with GP1b surface expression
enthalten in:
bioRxiv.org
| 2024
von
Campbell, I.
|
Crowley, T.
|
Jobaliya, C.
| +12
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2
Prenatal cardiac findings and 22q11.2 deletion syndrome : Fetal detection and evaluation
enthalten in:
Prenatal diagnosis
| 2024
von
Goldmuntz, E.
|
Bassett, A.
|
Boot, E.
| +8
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3
Prenatal detection of 22q11.2 deletion syndrome and congenital heart disease
enthalten in:
American journal of obstetrics and gynecology
| 2024
von
Freud, L.
|
Wapner, R.
|
McDonald-McGinn, D.
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4
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome
enthalten in:
bioRxiv.org
| 2024
von
Vervoort, L.
|
Dierckxsens, N.
|
Santos, M.
| +13
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5
Enlarged cavum septum pellucidum and small thymus as markers for 22q11.2 deletion syndrome
enthalten in:
Prenatal diagnosis
| 2024
von
Gaiser, K.
|
Schindewolf, E.
|
Conway, L.
| +8
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6
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome
enthalten in:
bioRxiv : the preprint server for biology
| 2024
von
Vervoort, L.
|
Dierckxsens, N.
|
Santos, M.
| +13
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7
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome : cardiac and noncardiac outcomes through 1 year of age
enthalten in:
American journal of obstetrics and gynecology
| 2024
von
Freud, L.
|
Galloway, S.
|
Crowley, T.
| +59
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8
A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgery
enthalten in:
Platelets
| 2024
von
Crowley, T.
|
Campbell, I.
|
Arulselvan, A.
| +7
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9
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS
enthalten in:
NPJ genomic medicine
| 2023
von
Zhao, Y.
|
Wang, Y.
|
Shi, L.
| +51
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10
Approaches to studying the impact of 22q11.2 copy number variants
enthalten in:
American journal of human genetics
| 2023
von
Bassett, A.
|
McDonald-McGinn, D.
|
Boot, E.
| +2
CommentOn: Am J Hum Genet. 2023 Feb 2;110(2):300-313. - PMID 36706759
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American journal of medical genetics. Part A
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