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1.
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
Am J Hum Genet
; 107(5): 932-941, 2020 11 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33108757
2.
Information-seeking preferences in diverse patients receiving a genetic testing result in the Clinical Sequencing Evidence-Generating Research (CSER) study.
Genet Med
; 25(9): 100899, 2023 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37212252
3.
Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods.
Genet Med
; 24(10): 2014-2027, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35833928
4.
Two patients with FOXF1 mutations with alveolar capillary dysplasia with misalignment of pulmonary veins and other malformations: Two different presentations and outcomes.
Am J Med Genet A
; 176(12): 2877-2881, 2018 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-30380203
5.
Lessons learned while starting multi-institutional genetics research in diverse populations: A report from the Clinical Sequencing Evidence-Generating Research (CSER) consortium.
Contemp Clin Trials
; 125: 107063, 2023 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-36567057
6.
Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience.
HGG Adv
; 3(3): 100120, 2022 Jul 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-35707062
7.
Osteoporosis in a Rural Community - Long-Term Effects of a Community Level Program of Calcium and Vitamin D Supplementation - A Prospective Observational Study.
Indian J Endocrinol Metab
; 25(4): 305-312, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-35136737
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