Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

314 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Genetic mapping of a second locus predisposing to hereditary non-polyposis colon cancer.
Lindblom A, Tannergård P, Werelius B, Nordenskjöld M. Lindblom A, et al. Among authors: nordenskjold m. Nat Genet. 1993 Nov;5(3):279-82. doi: 10.1038/ng1193-279. Nat Genet. 1993. PMID: 7903889
[Identification of cancer genes has made the testing of predisposition possible. Genetic counseling and mutation screening can result in new therapeutic methods].
Nordenskjöld M. Nordenskjöld M. Lakartidningen. 1999 Aug 11;96(32-33):3392-6. Lakartidningen. 1999. PMID: 10479788 Review. Swedish. No abstract available.
[Nobody will be punished for one's own hereditary disposition. Genetic information should be protected by law].
Lindblom A, Nordenskjöld M. Lindblom A, et al. Among authors: nordenskjold m. Lakartidningen. 1996 Mar 6;93(10):908-10. Lakartidningen. 1996. PMID: 8656797 Swedish. No abstract available.
[The gene of spinal muscular atrophy localized. Possibilities for prenatal diagnosis].
Blennow ES, Bui TH, Söderhäll S, Anvret M, Nordenskjöld M. Blennow ES, et al. Among authors: nordenskjold m. Lakartidningen. 1993 Jan 27;90(4):269-75. Lakartidningen. 1993. PMID: 8433608 Swedish. No abstract available.
[Families with hereditary cancer--a target group for prevention].
Lindblom A, Nordenskjöld M. Lindblom A, et al. Among authors: nordenskjold m. Lakartidningen. 1990 Nov 7;87(45):3775-8. Lakartidningen. 1990. PMID: 2233058 Swedish.
Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden.
Melin M, Entesarian M, Carlsson G, Garwicz D, Klein C, Fadeel B, Nordenskjöld M, Palmblad J, Henter JI, Dahl N. Melin M, et al. Among authors: nordenskjold m. Biochem Biophys Res Commun. 2007 Feb 16;353(3):571-5. doi: 10.1016/j.bbrc.2006.12.086. Epub 2006 Dec 20. Biochem Biophys Res Commun. 2007. PMID: 17188649 Free PMC article.
High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical setting.
Wincent J, Anderlid BM, Lagerberg M, Nordenskjöld M, Schoumans J. Wincent J, et al. Among authors: nordenskjold m. Clin Genet. 2011 Feb;79(2):147-57. doi: 10.1111/j.1399-0004.2010.01442.x. Clin Genet. 2011. PMID: 20486943
Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
Schoumans J, Ruivenkamp C, Holmberg E, Kyllerman M, Anderlid BM, Nordenskjöld M. Schoumans J, et al. Among authors: nordenskjold m. J Med Genet. 2005 Sep;42(9):699-705. doi: 10.1136/jmg.2004.029637. J Med Genet. 2005. PMID: 16141005 Free PMC article.
A high degree of aneuploidy in frozen-thawed human preimplantation embryos.
Iwarsson E, Lundqvist M, Inzunza J, Ahrlund-Richter L, Sjöblom P, Lundkvist O, Simberg N, Nordenskjöld M, Blennow E. Iwarsson E, et al. Among authors: nordenskjold m. Hum Genet. 1999 May;104(5):376-82. doi: 10.1007/s004390050971. Hum Genet. 1999. PMID: 10394928
Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
Göransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, Söderhäll C, Samuelsson A, Janka G, Schneider M, Gürgey A, Yalman N, Révész T, Egeler R, Jahnukainen K, Storm-Mathiesen I, Haraldsson A, Poole J, de Saint Basile G, Nordenskjöld M, Henter J. Göransdotter Ericson K, et al. Among authors: nordenskjold m. Am J Hum Genet. 2001 Mar;68(3):590-7. doi: 10.1086/318796. Epub 2001 Feb 6. Am J Hum Genet. 2001. PMID: 11179007 Free PMC article.
314 results
Jump to page
Feedback