Zobrazeno 1 - 10
of 307
pro vyhledávání: '"Ashkinadze, E."'
Autor:
Ricca J; Department of Oncology Services, Rutgers Cancer Institute of New Jersey at University Hospital, Newark, New Jersey, USA.; Rutgers University Genetic Counseling Master's Program, Piscataway, New Jersey, USA., Brandt JS; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, NYU Grossman School of Medicine, New York, New York, USA., Jacob N; PreventionGenetics LLC, Marshfield, Wisconsin, USA., Ashkinadze E; Rutgers University Genetic Counseling Master's Program, Piscataway, New Jersey, USA.; Department of Obstetrics, Gynecology, and Reproductive Sciences, Division of Maternal-Fetal Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Publikováno v:
Prenatal diagnosis [Prenat Diagn] 2024 Nov; Vol. 44 (12), pp. 1470-1478. Date of Electronic Publication: 2024 Mar 18.
Autor:
Roche K; Rutgers University Genetic Counseling Master's Program, New Brunswick, New Jersey, USA., Khan SP; Division of Maternal-Fetal Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Botti C; Division of Medical Genetics, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Giampietro P; Department of Pediatrics, University of Illinois College of Medicine, Chicago, Illinois, USA., Anderson S; Rutgers School of Nursing, Newark, New Jersey, USA., Ashkinadze E; Division of Maternal-Fetal Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Publikováno v:
Journal of genetic counseling [J Genet Couns] 2024 Oct; Vol. 33 (5), pp. 1026-1034. Date of Electronic Publication: 2023 Oct 25.
Autor:
Clevenger SK; Oncology Support Services, Morristown Medical Center, Morristown, New Jersey, USA.; Rutgers University Genetic Counseling Master's Program, Piscataway, New Jersey, USA., Brandt JS; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Khan SP; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Shingala P; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Carrick J; Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers, the State University of New Jersey, Piscataway, New Jersey, USA., Aluwalia R; Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers, the State University of New Jersey, Piscataway, New Jersey, USA., Heiman GA; Rutgers University Genetic Counseling Master's Program, Piscataway, New Jersey, USA.; Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers, the State University of New Jersey, Piscataway, New Jersey, USA., Ashkinadze E; Rutgers University Genetic Counseling Master's Program, Piscataway, New Jersey, USA.; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Publikováno v:
Prenatal diagnosis [Prenat Diagn] 2023 Jan; Vol. 43 (1), pp. 117-125. Date of Electronic Publication: 2023 Jan 03.
Autor:
Spinosi F; Department of Medical Genetics and Genomic Medicine, Saint Peter's University Hospital, New Brunswick, NJ, USA.; Rutgers University Genetic Counseling Master's Program, Piscataway, NJ, USA., Khan S; Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA., Seymour C; Rutgers University Genetic Counseling Master's Program, Piscataway, NJ, USA., Ashkinadze E; Rutgers University Genetic Counseling Master's Program, Piscataway, NJ, USA.; Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Publikováno v:
Journal of genetic counseling [J Genet Couns] 2021 Dec; Vol. 30 (6), pp. 1748-1756. Date of Electronic Publication: 2021 Jul 05.
Autor:
Temmesen, Camilla Gry1,2,3,4 (AUTHOR) ctemmesen@health.sdu.dk, Nielsen, Henriette Svarre5,6 (AUTHOR), Birch Petersen, Kathrine7 (AUTHOR), Clemensen, Jane2,3,4 (AUTHOR)
Publikováno v:
BMC Women's Health. 11/5/2024, Vol. 24 Issue 1, p1-13. 13p.
Autor:
Simone L; Hackensack University Medical Center, Hackensack, New Jersey, USA., Khan S; Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Ciarlariello M; Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Lin J; Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Trackman S; Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA., Heiman GA; Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers, the State University of New Jersey, Piscataway, New Jersey, USA., Ashkinadze E; Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Publikováno v:
Prenatal diagnosis [Prenat Diagn] 2021 Jan; Vol. 41 (1), pp. 21-27. Date of Electronic Publication: 2020 Sep 24.
Autor:
Dolitsky S; Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey., Mitra A; Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey., Khan S; Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey., Ashkinadze E; Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey., Sauer MV; Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey.
Publikováno v:
F&S reports [F S Rep] 2020 Aug 07; Vol. 1 (3), pp. 294-298. Date of Electronic Publication: 2020 Aug 07 (Print Publication: 2020).
Bardet-Biedl syndrome (BBS) is a rare pediatric ciliopathy characterized by marked clinical variability and extensive genetic heterogeneity. Typical diagnosis of BBS is secured at a median of 9 years of age, and sometimes well into adolescence. Here,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::854dbe5905f5190c843ad04f5a8d396f
https://europepmc.org/articles/PMC3638949/
https://europepmc.org/articles/PMC3638949/
Publikováno v:
Archives of Hellenic Medicine / Arheia Ellenikes Iatrikes. Sep/Oct2024, Vol. 41 Issue 5, p691-698. 8p.
Autor:
Piek, Steven R.1 (AUTHOR) steven.piek@ugent.be, Verghote, Kato1 (AUTHOR), Martani, Andrea2 (AUTHOR), Pennings, Guido1 (AUTHOR), Provoost, Veerle1 (AUTHOR)
Publikováno v:
PLoS ONE. 8/26/2024, Vol. 19 Issue 8, p1-17. 17p.