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Author/Creator Zarate, Yuri A.

12. Further supporting evidence for the SATB2‐associated syndrome found through whole exome sequencing. (May 2015)

Authors:
Zarate, Yuri A.; Perry, Hazel; Ben‐Omran, Tawfeg; Sellars, Elizabeth A.; Stein, Quinn; Almureikhi, Mariam; Simmons, Kirk; Klein, Ophir; Fish, Jennifer; Feingold, Murray; Douglas, Jessica; Kruer, Michael C.; Si, Yue; Mao, Rong; McKnight, Dianalee; Gibellini, Federica; Retterer, Kyle; Slavotinek, Anne
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 5(2015:May)
Page Start:
1026
Record Type:
Journal Article
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15. Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. Issue 4 (13th January 2021)

Authors:
Zarate, Yuri A.; Bosanko, Katherine A.; Thomas, Mary Ann; Miller, David T.; Cusmano‐Ozog, Kristina; Martinez‐Monseny, Antonio; Curry, Cynthia J.; Graham, John M.; Velsher, Lea; Bekheirnia, Mir Reza; Seidel, Veronica; Dedousis, Demitrios; Mitchell, Anna L.; DiMarino, Amy M.; Riess, Angelika; Balas...
Journal:
Clinical genetics
Issue:
Volume 99:Issue 4(2021)
Page Start:
547
Record Type:
Journal Article
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16. HIST1H1E heterozygous protein‐truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals. Issue 10 (9th August 2019)

Authors:
Burkardt, Deepika D'Cunha; Zachariou, Anna; Loveday, Chey; Allen, Clare L.; Amor, David J.; Ardissone, Anna; Banka, Siddharth; Bourgois, Alexia; Coubes, Christine; Cytrynbaum, Cheryl; Faivre, Laurence; Marion, Gerard; Horton, Rachel; Kotzot, Dieter; Lay‐Son, Guillermo; Lees, Melissa; Low, Karen; ...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 10(2019)
Page Start:
2049
Record Type:
Journal Article
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17. Introduction to the special issue on Clinical Genetics in Latin America. Issue 4 (22nd December 2020)

Authors:
Prada, Carlos E.; Cavalcanti, Denise; Schwartz, Ida Vanessa Doederlein; Zarate, Yuri A.
Other Names:
Prada Carlos E guestEditor.; Schwartz Ida guestEditor.; Cavalcanti Denise guestEditor.; Zarate Yuri A guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 184:Issue 4(2020)
Page Start:
873
Record Type:
Journal Article
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20. Mutation update for the SATB2 gene. Issue 8 (18th June 2019)

Authors:
Zarate, Yuri A.; Bosanko, Katherine A.; Caffrey, Aisling R.; Bernstein, Jonathan A.; Martin, Donna M.; Williams, Marc S.; Berry‐Kravis, Elizabeth M.; Mark, Paul R.; Manning, Melanie A.; Bhambhani, Vikas; Vargas, Marcelo; Seeley, Andrea H.; Estrada‐Veras, Juvianee I.; van Dooren, Marieke F.; Schwa...
Journal:
Human mutation
Issue:
Volume 40:Issue 8(2019)
Page Start:
1013
Record Type:
Journal Article
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