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Clinical genetics, 2024-08, Vol.106 (2), p.209-213
2024
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Human mutation, 2019-08, Vol.40 (8), p.1013-1029, Article humu.23771
- 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.
- Dooren, Marieke F.
- Schwab, Maria
- Vanderver, Adeline
- Melis, Daniela
- Alsadah, Adnan
- Sadler, Laurie
- Esch, Hilde
- Callewaert, Bert
- Oostra, Ann
- Maclean, Jane
- Dentici, Maria Lisa
- Orlando, Valeria
- Lipson, Mark
- Sparagana, Steven P.
- Maarup, Timothy J.
- Alsters, Suzanne IM
- Brautbar, Ariel
- Kovitch, Eliana
- Naidu, Sakkubai
- Lees, Melissa
- Smith, Douglas M.
- Turner, Lesley
- Raggio, Víctor
- Spangenberg, Lucía
- Garcia‐Miñaúr, Sixto
- Roeder, Elizabeth R.
- Littlejohn, Rebecca O.
- Grange, Dorothy
- Pfotenhauer, Jean
- Jones, Marilyn C.
- Balasubramanian, Meena
- Martinez‐Monseny, Antonio
- Blok, Lot Snijders
- Gavrilova, Ralitza
- Fish, Jennifer L.
2019
Link zum Volltext
American journal of medical genetics. Part A, 2023-07, Vol.191 (7), p.1984-1989
2023
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American journal of medical genetics. Part A, 2017-02, Vol.173 (2), p.327-337
2017
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Natural history and genotype‐phenotype correlations in 72 individuals with SATB2‐associated syndrome
- Zarate, Yuri A.
- Smith‐Hicks, Constance L.
- Greene, Carol
- Abbott, Mary‐Alice
- Siu, Victoria M.
- Calhoun, Amy R. U. L.
- Pandya, Arti
- Li, Chumei
- Sellars, Elizabeth A.
- Kaylor, Julie
- Bosanko, Katherine
- Kalsner, Louisa
- Basinger, Alice
- Slavotinek, Anne M.
- Perry, Hazel
- Saenz, Margarita
- Szybowska, Marta
- Wilson, Louise C.
- Kumar, Ajith
- Brain, Caroline
- Balasubramanian, Meena
- Dubbs, Holly
- Ortiz‐Gonzalez, Xilma R.
- Zackai, Elaine
- Stein, Quinn
- Powell, Cynthia M.
- Schrier Vergano, Samantha
- Britt, Allison
- Sun, Angela
- Smith, Wendy
- Bebin, E. Martina
- Picker, Jonathan
- Kirby, Amelia
- Pinz, Hailey
- Bombei, Hannah
- Mahida, Sonal
- Cohen, Julie S.
- Fatemi, Ali
- Vernon, Hilary J.
- McClellan, Rebecca
- Fleming, Leah R.
- Knyszek, Brittney
- Steinraths, Michelle
- Velasco Gonzalez, Cruz
- Beck, Anita E.
- Golden‐Grant, Katie L.
- Egense, Alena
- Parikh, Aditi
- Raimondi, Chantalle
- Angle, Brad
- Allen, William
- Schott, Suzanna
- Algrabli, Adi
- Robin, Nathaniel H.
- Ray, Joseph W.
- Everman, David B.
- Gambello, Michael J.
- Chung, Wendy K.
2018
Link zum Volltext
American journal of medical genetics. Part A, 2022-10, Vol.188 (10), p.2952-2957
2022
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American journal of medical genetics. Part A, 2021-08, Vol.185 (8), p.2391-2398
2021
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American journal of medical genetics. Part A, 2018-12, Vol.176 (12), p.2614-2622
2018
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Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2
- 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
- Balasubramanian, Meena
- Fish, Jennifer L.
- Caffrey, Aisling R.
- Fleischer, Nicole
- Pierson, Tyler Mark
- Lacro, Ronald V.
2021
Link zum Volltext
American journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.2168-2172
2022
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Clinical genetics, 2016-06, Vol.89 (6), p.728-732
2016
Link zum Volltext
Genes, brain and behavior, 2021-09, Vol.20 (7), p.e12761-n/a
2021
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Special care in dentistry, 2019-03, Vol.39 (2), p.220-224
2019
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Thema
- Life Sciences & Biomedicine
- Science & Technology
- Satb2-Associated Syndrome
- Satb2‐associated Syndrome
- Genetics & Heredity
- Humans
- Matrix Attachment Region Binding Proteins - Genetics
- Phenotypes
- Transcription Factors - Genetics
- Satb2
- Female
- Male
- Phenotype
- Syndrome
- Hereditary Diseases
- Neurodevelopmental Disorders
- Amino Acid Sequence
- Child
- Child, Preschool
- Abnormalities, Multiple - Genetics
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