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Human Genetics
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June 15, 2011
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions
Minire Hasi, Bridgette Soileau, Courtney Sebold, et al.
American Journal of Medical Genetics. Part A
|
January 15, 2015
Whole arm deletions of 18p: medical and developmental effects
Courtney Sebold, Bridgette Soileau, Patricia Heard, et al.
Journal of Genetic Counseling
|
November 19, 2014
Adults with Chromosome 18 Abnormalities
Bridgette Soileau, Minire Hasi, Courtney Sebold, et al.
American Journal of Medical Genetics. Part A
|
October 24, 2014
Ring 18 molecular assessment and clinical consequences
Erika Carter, Patricia Heard, Minire Hasi, et al.
Human Genetics
|
May 26, 2010
Genetic determinants of autism in individuals with deletions of 18q
Louise O'Donnell, Bridgette Soileau, Patricia Heard, et al.
Journal of Genetic Counseling
|
October 26, 2023
Understanding type and quality of relationships between individuals with chromosome 18 syndromes and their siblings
Catherine Cody Larson, Louise O'Donnell, Bridgette Soileau, et al.
Molecular Genetics & Genomic Medicine
|
April 1, 2018
The Chromosome 18 Clinical Resource Center
Jannine D Cody, Minire Hasi-Zogaj, Patricia Heard, et al.
American Journal of Medical Genetics. Part A
|
January 15, 2019
Abnormal bone mineral content and density in people with tetrasomy 18p
Alvaro Moreira, Hrishikesh Das, Minire Hasi-Zogaj, et al.
Human Genetics
|
October 5, 2013
Establishing a reference group for distal 18q-: clinical description and molecular basis
Jannine D Cody, Minire Hasi, Bridgette Soileau, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 4, 2015
Consequences of chromsome18q deletions
Jannine D Cody, Courtney Sebold, Patricia Heard, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Human Genetics
|
June 15, 2011
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions
Minire Hasi, Bridgette Soileau, Courtney Sebold, et al.
American Journal of Medical Genetics. Part A
|
January 15, 2015
Whole arm deletions of 18p: medical and developmental effects
Courtney Sebold, Bridgette Soileau, Patricia Heard, et al.
Journal of Genetic Counseling
|
November 19, 2014
Adults with Chromosome 18 Abnormalities
Bridgette Soileau, Minire Hasi, Courtney Sebold, et al.
American Journal of Medical Genetics. Part A
|
October 24, 2014
Ring 18 molecular assessment and clinical consequences
Erika Carter, Patricia Heard, Minire Hasi, et al.
Human Genetics
|
May 26, 2010
Genetic determinants of autism in individuals with deletions of 18q
Louise O'Donnell, Bridgette Soileau, Patricia Heard, et al.
Journal of Genetic Counseling
|
October 26, 2023
Understanding type and quality of relationships between individuals with chromosome 18 syndromes and their siblings
Catherine Cody Larson, Louise O'Donnell, Bridgette Soileau, et al.
Molecular Genetics & Genomic Medicine
|
April 1, 2018
The Chromosome 18 Clinical Resource Center
Jannine D Cody, Minire Hasi-Zogaj, Patricia Heard, et al.
American Journal of Medical Genetics. Part A
|
January 15, 2019
Abnormal bone mineral content and density in people with tetrasomy 18p
Alvaro Moreira, Hrishikesh Das, Minire Hasi-Zogaj, et al.
Human Genetics
|
October 5, 2013
Establishing a reference group for distal 18q-: clinical description and molecular basis
Jannine D Cody, Minire Hasi, Bridgette Soileau, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 4, 2015
Consequences of chromsome18q deletions
Jannine D Cody, Courtney Sebold, Patricia Heard, et al.
Page
of 2