Publications | Lund University Publications

271 – 280 of 305

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/publication?embed=1&q=keywords+exact+%22Mutation%22&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

1999
Mark Cancer risks in BRCA2 mutation carriers
Olsson, Håkan ^LU (1999) In Journal of the National Cancer Institute 91(15). p.6-1310
- Contribution to journal › Article
Mark Search for MODY and Type 2 diabetes genes
Lehto, Markku ^LU (1999)
- Thesis › Doctoral thesis (compilation)
1998
Mark Analysis of Swedish male breast cancer family data : a simple way to incorporate a common sibling effect
Karunaratne, P M ; Elston, R C ; Loman, N ^LU ; Olsson, H ^LU and Ranstam, J ^LU (1998) In Genetic Epidemiology 15(2). p.12-201
- Contribution to journal › Article
Mark BRCA1-positive patients are small for gestational age compared with their unaffected relatives
Jernström, H ^LU ; Johannsson, O ^LU ; Borg, A ^LU ; Ivarsson, H and Olsson, H ^LU (1998) In European Journal of Cancer 34(3). p.71-368
- Contribution to journal › Article
Mark Mutations in the low-density lipoprotein receptor gene in Swedish familial hypercholesterolaemia patients: clinical expression and treatment response
Ekström, Ulf ^LU ; Abrahamson, Magnus ^LU ; Wallmark, Anders ^LU ; Florén, Claes-Henrik ^LU and Nilsson-Ehle, Peter ^LU (1998) In European Journal of Clinical Investigation 28(9). p.740-747
- Contribution to journal › Article
Mark Detection of alterations in all three exons of the peripherin/RDS gene in Swedish patients with retinitis pigmentosa using an efficient DGGE system
Ekström, Ulf ^LU ; Ponjavic, Vesna ^LU ; Andréasson, Sten ^LU ; Ehinger, Berndt ^LU ; Nilsson-Ehle, Peter ^LU and Abrahamson, Magnus ^LU (1998) In Molecular Pathology 51(5). p.287-291
- Contribution to journal › Article
Mark Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course
Holinski-Feder, E ; Weiss, M ; Brandau, O ; Jedele, KB ; Nore, B ; Backesjo, CM ; Vihinen, Mauno ^LU ; Hubbard, SR ; Belohradsky, BH and Smith, CIE , et al. (1998) In Pediatrics 101(2). p.276-284
- Contribution to journal › Article
Mark Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect
Simmonds, R E ; Ireland, H ; Lane, D A ; Zöller, B ^LU ; García de Frutos, P and Dahlbäck, B ^LU (1998) In Annals of Internal Medicine 128(1). p.8-14
- Contribution to journal › Article
Mark Caracterización genómica de la cepa cubana de efecto citopático ligero
Alvarez Vera, M ; Sarmiento Pérez, L ^LU ; Guzmán Tirado, M G ; Beck, M ; Shi, Q ; Handy, J and Más Lago, P (1998) In Revista cubana de medicina tropical 50(suppl 1). p.9-267
- Contribution to journal › Article
Mark Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism
Carling, T ; Correa, Pamela ; Hessman, O ; Hedberg, J ; Skogseid, B ; Lindberg, D ^LU ; Rastad, J ; Westin, G and Akerström, G (1998) In The Journal of clinical endocrinology and metabolism 83(8). p.2960-2963
- Contribution to journal › Article

your query:: Remove keywords: Mutation