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Katherine A Bosanko

Showing results (1-10 of 15) with videos related to

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Journal of Human Genetics|September 26, 2019
Using facial analysis technology in a typical genetic clinic: experience from 30 individuals from a single institutionYuri A Zarate, Katherine A Bosanko, Karen W Gripp
American Journal of Medical Genetics. Part A|May 10, 2021
SATB2-associated syndrome in adolescents and adultsYuri A Zarate, Katherine A Bosanko, Aisling R Caffrey
American Journal of Medical Genetics. Part A|July 15, 2022
Growth in individuals with SATB2-associated syndromeYuri A Zarate, Amrit Kannan, Katherine A Bosanko, et al.
Case Reports in Pediatrics|July 16, 2014
Description of the first case of adenomyomatosis of the gallbladder in an infantYuri A Zarate, Katherine A Bosanko, Chaowapong Jarasvaraparn, et al.
Seminars in Pediatric Neurology|August 24, 2014
A newborn with complex skeletal abnormalities, joint contractures, and bilateral corneal clouding with sclerocorneaElizabeth A Sellars, Katherine A Bosanko, Tiffany Lepard, et al.
American Journal of Medical Genetics. Part A|November 22, 2017
Less common underlying genetic diagnoses found in a cohort of 139 individuals surgically corrected for craniosynostosisBenjamin R Ittleman, Jasmine Mckissick, Katherine A Bosanko, et al.
American Journal of Medical Genetics. Part A|April 28, 2015
Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnosesYuri A Zarate, Katherine A Bosanko, Elizabeth Bhoj, et al.
Frontiers in Genetics|July 8, 2021
Case Report: <i>SATB2</i>-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two CasesYuri A Zarate, Hilary J Vernon, Katherine A Bosanko, et al.
Journal of Medical Genetics|September 26, 2024
Pathogenic <i>SATB2</i> missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypesJoery den Hoed, Hirokazu Hashimoto, Mubeen Khan, et al.
Clinical Genetics|December 31, 2020
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2Yuri A Zarate, Katherine A Bosanko, Mary Ann Thomas, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Human Genetics|September 26, 2019
Using facial analysis technology in a typical genetic clinic: experience from 30 individuals from a single institutionYuri A Zarate, Katherine A Bosanko, Karen W Gripp
American Journal of Medical Genetics. Part A|May 10, 2021
SATB2-associated syndrome in adolescents and adultsYuri A Zarate, Katherine A Bosanko, Aisling R Caffrey
American Journal of Medical Genetics. Part A|July 15, 2022
Growth in individuals with SATB2-associated syndromeYuri A Zarate, Amrit Kannan, Katherine A Bosanko, et al.
Case Reports in Pediatrics|July 16, 2014
Description of the first case of adenomyomatosis of the gallbladder in an infantYuri A Zarate, Katherine A Bosanko, Chaowapong Jarasvaraparn, et al.
Seminars in Pediatric Neurology|August 24, 2014
A newborn with complex skeletal abnormalities, joint contractures, and bilateral corneal clouding with sclerocorneaElizabeth A Sellars, Katherine A Bosanko, Tiffany Lepard, et al.
American Journal of Medical Genetics. Part A|November 22, 2017
Less common underlying genetic diagnoses found in a cohort of 139 individuals surgically corrected for craniosynostosisBenjamin R Ittleman, Jasmine Mckissick, Katherine A Bosanko, et al.
American Journal of Medical Genetics. Part A|April 28, 2015
Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnosesYuri A Zarate, Katherine A Bosanko, Elizabeth Bhoj, et al.
Frontiers in Genetics|July 8, 2021
Case Report: <i>SATB2</i>-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two CasesYuri A Zarate, Hilary J Vernon, Katherine A Bosanko, et al.
Journal of Medical Genetics|September 26, 2024
Pathogenic <i>SATB2</i> missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypesJoery den Hoed, Hirokazu Hashimoto, Mubeen Khan, et al.
Clinical Genetics|December 31, 2020
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2Yuri A Zarate, Katherine A Bosanko, Mary Ann Thomas, et al.
Pageof 2