Nordling M - Search Results

1

PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families.

Bjursell C, Erlandson A, Nordling M, Nilsson S, Wahlström J, Stibler H, Kristiansson B, Martinsson T. Bjursell C, et al. Among authors: nordling m. Hum Mutat. 2000 Nov;16(5):395-400. doi: 10.1002/1098-1004(200011)16:5<395::AID-HUMU3>3.0.CO;2-T. Hum Mutat. 2000. PMID: 11058896

2

[von Hippel-Lindau hereditary tumor syndrome. Mutational analysis may improve prognosis].

Wiklund L, Nordling M, Engwall Y, Martinsson T, Szentgyörgyi E, Wahlström J. Wiklund L, et al. Among authors: nordling m. Lakartidningen. 1995 Mar 15;92(11):1093-6. Lakartidningen. 1995. PMID: 7700111 Swedish.

3

Novel mutations in the APC gene and clinical features in Swedish patients with polyposis coli.

Nordling M, Engwall Y, Wahlström J, Wiklund L, Eriksson MA, Gustavsson B, Fasth S, Larsson PA, Martinsson T. Nordling M, et al. Anticancer Res. 1997 Nov-Dec;17(6D):4275-80. Anticancer Res. 1997. PMID: 9494520

4

Delimitation of a critical tumour suppressor region at distal 1p in neuroblastoma tumours.

Martinsson T, Sjöberg RM, Hallstensson K, Nordling M, Hedborg F, Kogner P. Martinsson T, et al. Among authors: nordling m. Eur J Cancer. 1997 Oct;33(12):1997-2001. doi: 10.1016/s0959-8049(97)00278-5. Eur J Cancer. 1997. PMID: 9516841

5

A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family.

Nordling M, Karlsson P, Wahlström J, Engwall Y, Wallgren A, Martinsson T. Nordling M, et al. Cancer Res. 1998 Apr 1;58(7):1372-5. Cancer Res. 1998. PMID: 9537232

6

A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer.

Einbeigi Z, Bergman A, Kindblom LG, Martinsson T, Meis-Kindblom JM, Nordling M, Suurküla M, Wahlström J, Wallgren A, Karlsson P. Einbeigi Z, et al. Among authors: nordling m. Eur J Cancer. 2001 Oct;37(15):1904-9. doi: 10.1016/s0959-8049(01)00223-4. Eur J Cancer. 2001. PMID: 11576847

7

Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutations.

Björk J, Akerbrant H, Iselius L, Bergman A, Engwall Y, Wahlström J, Martinsson T, Nordling M, Hultcrantz R. Björk J, et al. Among authors: nordling m. Gastroenterology. 2001 Nov;121(5):1127-35. doi: 10.1053/gast.2001.28707. Gastroenterology. 2001. PMID: 11677205

8

The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation.

Bergman A, Einbeigi Z, Olofsson U, Taib Z, Wallgren A, Karlsson P, Wahlström J, Martinsson T, Nordling M. Bergman A, et al. Among authors: nordling m. Eur J Hum Genet. 2001 Oct;9(10):787-93. doi: 10.1038/sj.ejhg.5200704. Eur J Hum Genet. 2001. PMID: 11781691

9

Identification of genomic deletions of the APC gene in familial adenomatous polyposis by two independent quantitative techniques.

Meuller J, Kanter-Smoler G, Nygren AO, Errami A, Grönberg H, Holmberg E, Björk J, Wahlström J, Nordling M. Meuller J, et al. Among authors: nordling m. Genet Test. 2004 Fall;8(3):248-56. doi: 10.1089/gte.2004.8.248. Genet Test. 2004. PMID: 15727247

10

A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques.

Bergman A, Flodin A, Engwall Y, Arkblad EL, Berg K, Einbeigi Z, Martinsson T, Wahlström J, Karlsson P, Nordling M. Bergman A, et al. Among authors: nordling m. Fam Cancer. 2005;4(2):89-96. doi: 10.1007/s10689-004-5812-2. Fam Cancer. 2005. PMID: 15951958

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