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Prenatal Diagnosis
|
December 13, 2024
Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort
Federica Ruscitti, Tara Giacchino, Lemonia Koutoulas, et al.
Neurobiology of Aging
|
January 10, 2013
Brain structure in asymptomatic FMR1 premutation carriers at risk for fragile X-associated tremor/ataxia syndrome
Giovanni Battistella, Julien Niederhauser, Eleonora Fornari, et al.
American Journal of Medical Genetics. Part A
|
October 15, 2013
Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci
Livia Garavelli, Maria Rosaria Piemontese, Alberto Cavazza, et al.
European Journal of Human Genetics : EJHG
|
August 18, 2022
Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
March 14, 2022
Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
July 28, 2011
Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome
Peter Hammond, Femke Hannes, Michael Suttie, et al.
European Journal of Pediatrics
|
May 18, 2010
Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis
Faustina Lalatta, Donatella Quagliarini, Emanuela Folliero, et al.
European Journal of Human Genetics : EJHG
|
November 30, 2022
Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
December 19, 2022
Correction to: Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
June 21, 2012
Developing a policy for paediatric biobanks: principles for good practice
Kristien Hens, Carla E Van El, Pascal Borry, et al.
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Search research articles
Search
Showing results (31-40 of 77) with videos related to
Sort By:
Page
of 8
Prenatal Diagnosis
|
December 13, 2024
Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort
Federica Ruscitti, Tara Giacchino, Lemonia Koutoulas, et al.
Neurobiology of Aging
|
January 10, 2013
Brain structure in asymptomatic FMR1 premutation carriers at risk for fragile X-associated tremor/ataxia syndrome
Giovanni Battistella, Julien Niederhauser, Eleonora Fornari, et al.
American Journal of Medical Genetics. Part A
|
October 15, 2013
Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci
Livia Garavelli, Maria Rosaria Piemontese, Alberto Cavazza, et al.
European Journal of Human Genetics : EJHG
|
August 18, 2022
Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
March 14, 2022
Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
July 28, 2011
Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome
Peter Hammond, Femke Hannes, Michael Suttie, et al.
European Journal of Pediatrics
|
May 18, 2010
Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis
Faustina Lalatta, Donatella Quagliarini, Emanuela Folliero, et al.
European Journal of Human Genetics : EJHG
|
November 30, 2022
Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
December 19, 2022
Correction to: Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
Francesca Forzano, Olga Antonova, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
June 21, 2012
Developing a policy for paediatric biobanks: principles for good practice
Kristien Hens, Carla E Van El, Pascal Borry, et al.
Page
of 8