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Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.
Hum Genet. 1991 Mar;86(5):481-3. doi: 10.1007/BF00194637.
Hum Genet. 1991.
PMID: 2016087
A normal male with an inherited deletion of one exon within the DMD gene.
Nordenskjöld M, Nicholson L, Edström L, Anvret M, Eiserman M, Slater C, Stolpe L.
Nordenskjöld M, et al. Among authors: stolpe l.
Hum Genet. 1990 Jan;84(2):207-9. doi: 10.1007/BF00208944.
Hum Genet. 1990.
PMID: 2404853
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Characterization of the frequency of delta F508 mutation and CF haplotypes in Swedish families.
Anvret M, Stolpe L, Dahl N, Eiserman M, Nordenskjöld M, Starborg M, Johansson L.
Anvret M, et al. Among authors: stolpe l.
Clin Genet. 1991 Mar;39(3):238-9. doi: 10.1111/j.1399-0004.1991.tb03019.x.
Clin Genet. 1991.
PMID: 1709843
No abstract available.
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394delTT: a Nordic cystic fibrosis mutation.
Schwartz M, Anvret M, Claustres M, Eiken HG, Eiklid K, Schaedel C, Stolpe L, Tranebjaerg L.
Schwartz M, et al. Among authors: stolpe l.
Hum Genet. 1994 Feb;93(2):157-61. doi: 10.1007/BF00210602.
Hum Genet. 1994.
PMID: 7509310
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Frequency of four cystic fibrosis mutations in a Swedish population.
Dahl N, Grandell U, Martinsson T, Allen M, Johansson L, Stolpe L, Gyllensten U, Hjelte L, Kollberg H, Strandvik B, et al.
Dahl N, et al. Among authors: stolpe l.
Acta Paediatr. 1993 Jun-Jul;82(6-7):609. doi: 10.1111/j.1651-2227.1993.tb12769.x.
Acta Paediatr. 1993.
PMID: 8339003
No abstract available.
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The trophoblastic epithelial barrier is not infected in full-term placentae of human immunodeficiency virus-seropositive mothers undergoing antiretroviral therapy.
Tscherning-Casper C, Papadogiannakis N, Anvret M, Stolpe L, Lindgren S, Bohlin AB, Albert J, Fenyö EM.
Tscherning-Casper C, et al. Among authors: stolpe l.
J Virol. 1999 Nov;73(11):9673-8. doi: 10.1128/JVI.73.11.9673-9678.1999.
J Virol. 1999.
PMID: 10516083
Free PMC article.
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