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Author/Creator Lin, Angela E.

1. "Donating our bodies to science": A discussion about autopsy and organ donation in Turner syndrome. Issue 1 (11th January 2019)

Authors:
Prakash, Siddharth K.; San Roman, Adrianna K.; Crenshaw, Melissa; Flink, Barbara; Earle, Kimberly; Los, Evan; Bonnard, Åsa; Lin, Angela E.
Other Names:
Kruszka Paul guestEditor.; Silberbach Michael guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 181:Issue 1(2019)
Page Start:
22
Record Type:
Journal Article
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2. Alternatives to Autopsy for Fetal and Early Neonatal (Perinatal) Deaths: Insights from the Wisconsin Stillbirth Service Program. Issue 18 (12th September 2017)

Authors:
McPherson, Elspeth; Nestoridi, Eirini; Heinke, Dominique; Roberts, Drucilla J.; Fretts, Ruth; Yazdy, Mahsa M.; Lin, Angela E.
Other Names:
Kirby Russell guestEditor.; Browne Marilyn guestEditor.
Journal:
Birth defects research
Issue:
Volume 109:Issue 18(2017)
Page Start:
1430
Record Type:
Journal Article
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3. An additional patient with SMAD4‐Juvenile Polyposis‐Hereditary hemorrhagic telangiectasia and connective tissue abnormalities: SMAD4 loss‐of‐function and gain‐of‐function pathogenic variants result in contrasting phenotypes. Issue 10 (23rd July 2022)

Authors:
Gheewalla, Gregory M.; Luther, Jay; Das, Saumya; Kreher, Jeffrey B.; Scimone, Eleanor R.; Wong, Ashley W.; Lindsay, Mark E.; Lin, Angela E.
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 10(2022)
Page Start:
3084
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. An application of data mining to identify potential risk factors for anophthalmia and microphthalmia. Issue 6 (9th October 2018)

Authors:
Weber, Kari A.; Yang, Wei; Carmichael, Suzan L.; Lupo, Philip J.; Dukhovny, Stephanie; Yazdy, Mahsa M.; Lin, Angela E.; Van Bennekom, Carla M.; Mitchell, Allen A.; Shaw, Gary M.
Journal:
Paediatric and perinatal epidemiology
Issue:
Volume 32:Issue 6(2018:Nov.)
Page Start:
545
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry. Issue 12 (8th September 2016)

Authors:
Prakash, Siddharth K.; Bondy, Carolyn A.; Maslen, Cheryl L.; Silberbach, Michael; Lin, Angela E.; Perrone, Laura; Limongelli, Giuseppe; Michelena, Hector I.; Bossone, Eduardo; Citro, Rodolfo; Lemaire, Scott A.; Body, Simon C.; Milewicz, Dianna M.
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 12(2016)
Page Start:
3157
Record Type:
Journal Article
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7. Cardiac transplantation in children with Noonan syndrome. (1st July 2019)

Authors:
McCallen, Leslie M.; Ameduri, Rebecca K.; Denfield, Susan W.; Dodd, Debra A.; Everitt, Melanie D.; Johnson, Jonathan N.; Lee, Teresa M.; Lin, Angela E.; Lohr, Jamie L.; May, Lindsay J.; Pierpont, Mary Ella; Stevenson, David A.; Chatfield, Kathryn C.
Journal:
Pediatric transplantation
Issue:
Volume 23:Number 6(2019)
Page Start:
n/a
Record Type:
Journal Article
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9. Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome. (4th March 2023)

Authors:
Hoyek, Sandra; Wang, Marlene; Berrocal, Audina M.; Wong, Ashley; Place, Emily M.; Mason-Suares, Heather; Lin, Angela E.; Mukai, Shizuo; Patel, Nimesh A.
Journal:
Ophthalmic genetics
Issue:
Volume 44:Number 2(2023)
Page Start:
198
Record Type:
Journal Article
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10. Congenital heart defects associated with aneuploidy syndromes: New insights into familiar associations. Issue 1 (23rd December 2019)

Authors:
Lin, Angela E.; Santoro, Stephanie; High, Frances A.; Goldenberg, Paula; Gutmark‐Little, Iris
Other Names:
Kruszka Paul guestEditor.; Beaton Andrea guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 184:Issue 1(2020)
Page Start:
53
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗