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Best Practice & Research. Clinical Obstetrics & Gynaecology|December 12, 2002
Prenatal diagnosis: molecular genetics and cytogeneticsThe-Hung Bui, Elisabeth Blennow, Magnus Nordenskjöld
Lakartidningen|October 5, 2002
[New analytic methods provide answers regarding chromosome aberrations in 1-2 days]The-Hung Bui, Elisabeth Blennow, Magnus Nordenskjöld
Nature Genetics|May 7, 2025
Toward clinical long-read genome sequencing for rare diseasesJesper Eisfeldt, Marlene Ek, Magnus Nordenskjöld, et al.
American Journal of Medical Genetics. Part A|February 11, 2005
Detailed clinical description of four patients with 1.3 and 2.1 Mb chromosome imbalances derived from a familial t(12;17)(q24.33;q25.3)Jacqueline Schoumans, Gunnar Sanner, Magnus Nordenskjöld, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 23, 2021
Kostmann disease and other forms of severe congenital neutropeniaBengt Fadeel, Daniel Garwicz, Göran Carlsson, et al.
Nature Genetics|July 10, 2007
Bi-orientation of achiasmatic chromosomes in meiosis I oocytes contributes to aneuploidy in miceAnna Kouznetsova, Lisa Lister, Magnus Nordenskjöld, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 12, 2012
Ovarian failure in HAX1-deficient patients: is there a gender-specific difference in pubertal development in severe congenital neutropenia or Kostmann disease?Göran Carlsson, Berit Kriström, Magnus Nordenskjöld, et al.
Neuroendocrinology|May 13, 2010
First report on metastasizing small bowel carcinoids in first-degree relatives in three generationsJohannes Järhult, Kalle Landerholm, Sture Falkmer, et al.
Journal of Genetic Counseling|August 3, 2016
Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in SwedenSusanne Georgsson, Ellika Sahlin, Moa Iwarsson, et al.
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