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American Journal of Medical Genetics. Part A
|
July 22, 2014
Radiographic evaluation of stillbirth: what does it contribute?
Erica Swenson, Lynn Schema, Elizabeth McPherson
Journal of Medical Case Reports
|
January 26, 2021
Genetic developmental disability diagnosed in adulthood: a case report
Adam Langenfeld, Lynn Schema, Judith K Eckerle
American Journal of Medical Genetics. Part A
|
October 24, 2014
Neuroblastoma in a 17-week fetus: a stimulus for investigation of tumors in a series of 2786 stillbirth and late miscarriages
Elizabeth McPherson, Christopher Cold, Peter Johnson, et al.
Journal of Genetic Counseling
|
February 6, 2015
Clearing the Air: A Qualitative Investigation of Genetic Counselors' Experiences of Counselor-Focused Patient Anger
Lynn Schema, Michaela McLaughlin, Patricia McCarthy Veach, et al.
Journal of Genetic Counseling
|
May 3, 2021
Genetic counselor use of self-involving responses in a clinical setting: A qualitative investigation
Iman Kashmola-Perez, Patricia McCarthy Veach, Lynn Schema, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2021
Rare presentation of FDX2-related disorder and untargeted global metabolomics findings
Anjali Aggarwal, Nishitha R Pillai, Charles J Billington, et al.
Journal of Genetic Counseling
|
September 13, 2021
Differences in genetic counseling student responses to intense patient affect: A study of students in North American programs
Rachel Keppers, Patricia McCarthy Veach, Lynn Schema, et al.
Molecular Genetics and Metabolism
|
May 7, 2017
Infantile gangliosidoses: Mapping a timeline of clinical changes
Jeanine R Jarnes Utz, Sarah Kim, Kelly King, et al.
Case Reports in Endocrinology
|
June 8, 2026
21-Hydroxylase Deficient Congenital Adrenal Hyperplasia Due to Maternal Uniparental Isodisomy
Michelle L Kluge, Lynn Schema, Katy Schroepfer, et al.
American Journal of Human Genetics
|
April 17, 2018
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia
Claire Guissart, Xenia Latypova, Paul Rollier, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
American Journal of Medical Genetics. Part A
|
July 22, 2014
Radiographic evaluation of stillbirth: what does it contribute?
Erica Swenson, Lynn Schema, Elizabeth McPherson
Journal of Medical Case Reports
|
January 26, 2021
Genetic developmental disability diagnosed in adulthood: a case report
Adam Langenfeld, Lynn Schema, Judith K Eckerle
American Journal of Medical Genetics. Part A
|
October 24, 2014
Neuroblastoma in a 17-week fetus: a stimulus for investigation of tumors in a series of 2786 stillbirth and late miscarriages
Elizabeth McPherson, Christopher Cold, Peter Johnson, et al.
Journal of Genetic Counseling
|
February 6, 2015
Clearing the Air: A Qualitative Investigation of Genetic Counselors' Experiences of Counselor-Focused Patient Anger
Lynn Schema, Michaela McLaughlin, Patricia McCarthy Veach, et al.
Journal of Genetic Counseling
|
May 3, 2021
Genetic counselor use of self-involving responses in a clinical setting: A qualitative investigation
Iman Kashmola-Perez, Patricia McCarthy Veach, Lynn Schema, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2021
Rare presentation of FDX2-related disorder and untargeted global metabolomics findings
Anjali Aggarwal, Nishitha R Pillai, Charles J Billington, et al.
Journal of Genetic Counseling
|
September 13, 2021
Differences in genetic counseling student responses to intense patient affect: A study of students in North American programs
Rachel Keppers, Patricia McCarthy Veach, Lynn Schema, et al.
Molecular Genetics and Metabolism
|
May 7, 2017
Infantile gangliosidoses: Mapping a timeline of clinical changes
Jeanine R Jarnes Utz, Sarah Kim, Kelly King, et al.
Case Reports in Endocrinology
|
June 8, 2026
21-Hydroxylase Deficient Congenital Adrenal Hyperplasia Due to Maternal Uniparental Isodisomy
Michelle L Kluge, Lynn Schema, Katy Schroepfer, et al.
American Journal of Human Genetics
|
April 17, 2018
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia
Claire Guissart, Xenia Latypova, Paul Rollier, et al.
Page
of 1