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Author/Creator MacDonald, Alexandra

1. "Strength at Home" Intervention for Male Veterans Perpetrating Intimate Partner Aggression: Perceived Needs Survey of Therapists and Pilot Effectiveness Study. (August 2015)

Authors:
Love, Allison R.; Morland, Leslie A.; Menez, Ursula; Taft, Casey; MacDonald, Alexandra; Mackintosh, Margaret-Anne
Journal:
Journal of interpersonal violence
Issue:
Volume 30:Number 13(2015)
Page Start:
2344
Record Type:
Journal Article
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2. A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with marden–walker syndrome. Issue 9 (25th July 2013)

Authors:
Carrascosa‐Romero, María Carmen; Suela, Javier; Pardal‐Fernández, José Manuel; Bermejo‐Sánchez, Eva; Vidal‐Company, Alberto; MacDonald, Alexandra; Tébar‐Gil, Roque; Martínez‐Fernández, María Luisa; Martínez‐Frías, María Luisa
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 9(2013:Sep.)
Page Start:
2281
Record Type:
Journal Article
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3. A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with marden–walker syndrome. Issue 9 (25th July 2013)

Authors:
Carrascosa‐Romero, María Carmen; Suela, Javier; Pardal‐Fernández, José Manuel; Bermejo‐Sánchez, Eva; Vidal‐Company, Alberto; MacDonald, Alexandra; Tébar‐Gil, Roque; Martínez‐Fernández, María Luisa; Martínez‐Frías, María Luisa
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 9(2013:Sep.)
Page Start:
2281
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Deletion 1q43‐44 in a patient with clinical diagnosis of Warburg–Micro syndrome. (21st April 2015)

Authors:
Arroyo‐Carrera, Ignacio; de Zaldívar Tristancho, María Solo; Bermejo‐Sánchez, Eva; Martínez‐Fernández, María Luisa; López‐Lafuente, Amparo; MacDonald, Alexandra; Zúñiga, Ángel; Luis Gómez‐Skarmeta, José; Luisa Martínez‐Frías, María
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 6(2015:Jun.)
Page Start:
1243
Record Type:
Journal Article
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6. Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date. (21st April 2015)

Authors:
Martínez‐Fernández, María Luisa; Fernández‐Toral, Joaquin; Llano‐Rivas, Isabel; Bermejo‐Sánchez, Eva; MacDonald, Alexandra; Martínez‐Frías, María Luisa
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 9(2015:Sep.)
Page Start:
2034
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

7. Haploinsufficiency of BMP4 gene may be the underlying cause of Frías syndrome. Issue 2 (5th December 2013)

Authors:
Martínez‐Fernández, María Luisa; Bermejo‐Sánchez, Eva; Fernández, Belén; MacDonald, Alexandra; Fernández‐Toral, Joaquín; Martínez‐Frías, María Luisa
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 2(2014.)
Page Start:
338
Record Type:
Journal Article
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8. Interstitial deletion 14q22.3‐q23.2: Genotype–phenotype correlation. Issue 3 (19th December 2013)

Authors:
Martínez‐Frías, María Luisa; Ocejo‐Vinyals, Javier Gonzalo; Arteaga, Rosa; Martínez‐Fernández, María Luisa; MacDonald, Alexandra; Pérez‐Belmonte, Elena; Bermejo‐Sánchez, Eva; Martínez, Salvador
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 3(2014.)
Page Start:
639
Record Type:
Journal Article
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