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Journal of Genetic Counseling|November 19, 2014
A Genetic Lung Cancer Susceptibility Test may have a Positive Effect on Smoking CessationTammy Kammin, Andrew K Fenton, Kathryn Thirlaway
European Journal of Human Genetics : EJHG|January 12, 2018
Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatinCinthya J Zepeda-Mendoza, Alexandra Bardon, Tammy Kammin, et al.
European Journal of Human Genetics : EJHG|March 28, 2023
Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, SheffieldJessica M Bowen, Monica Hernandez, Diana S Johnson, et al.
American Journal of Human Genetics|December 24, 2019
SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male InfertilitySamantha L P Schilit, Shreya Menon, Corinna Friedrich, et al.
Journal of Clinical Periodontology|July 14, 2022
Oral characteristics in adult individuals with periodontal Ehlers-Danlos syndromeUlrike Lepperdinger, Chloe Angwin, Di Milnes, et al.
Human Molecular Genetics|January 14, 2016
Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis†Kusumika Mukherjee, Kana Ishii, Vamsee Pillalamarri, et al.
Journal of Community Genetics|March 9, 2023
An exemplary model of genetic counselling for highly specialised servicesJuliette Harris, Marion Bartlett, Duncan Baker, et al.
European Journal of Human Genetics : EJHG|July 7, 2016
Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delaySamantha Lp Schilit, Benjamin B Currall, Ruen Yao, et al.
American Journal of Human Genetics|July 25, 2017
Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal RearrangementsCinthya J Zepeda-Mendoza, Jonas Ibn-Salem, Tammy Kammin, et al.
American Journal of Human Genetics|October 18, 2016
Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal DiagnosisZehra Ordulu, Tammy Kammin, Harrison Brand, et al.
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