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Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis.
de la Chapelle A, Sankila EM, Lindlöf M, Aula P, Norio R. de la Chapelle A, et al. Among authors: lindlof m. Clin Genet. 1985 Oct;28(4):317-20. doi: 10.1111/j.1399-0004.1985.tb00405.x. Clin Genet. 1985. PMID: 2998655
Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
Kääriäinen H, Lindlöf M, Somer H, de la Chapelle A. Kääriäinen H, et al. Among authors: lindlof m. Clin Genet. 1990 Mar;37(3):179-87. doi: 10.1111/j.1399-0004.1990.tb03500.x. Clin Genet. 1990. PMID: 1969777
Gene deletions in X-linked muscular dystrophy.
Lindlöf M, Kiuru A, Kääriäinen H, Kalimo H, Lang H, Pihko H, Rapola J, Somer H, Somer M, Savontaus ML, et al. Lindlöf M, et al. Am J Hum Genet. 1989 Apr;44(4):496-503. Am J Hum Genet. 1989. PMID: 2929594 Free PMC article.
Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
Lindlöf M, Kääriäinen H, Davies KE, de la Chapelle A. Lindlöf M, et al. J Med Genet. 1986 Dec;23(6):560-72. doi: 10.1136/jmg.23.6.560. J Med Genet. 1986. PMID: 2879928 Free PMC article.
Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations.
Lindlöf M, Kääriäinen H, van Ommen GJ, de la Chapelle A. Lindlöf M, et al. Clin Genet. 1988 Feb;33(2):131-9. doi: 10.1111/j.1399-0004.1988.tb03424.x. Clin Genet. 1988. PMID: 3162851
Prenatal diagnosis of X-linked chronic granulomatous disease using restriction fragment length polymorphism analysis.
Lindlöf M, Kere J, Ristola M, Repo H, Leirisalo-Repo M, von Koskull H, Ammälä P, de la Chapelle A. Lindlöf M, et al. Genomics. 1987 Sep;1(1):87-92. doi: 10.1016/0888-7543(87)90109-1. Genomics. 1987. PMID: 2889663
Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.
Saviranta P, Lindlöf M, Lehesjoki AE, Kalimo H, Lang H, Sonninen V, Savontaus ML, de la Chapelle A. Saviranta P, et al. Among authors: lindlof m. Am J Hum Genet. 1988 Jan;42(1):84-8. Am J Hum Genet. 1988. PMID: 2892402 Free PMC article.
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM. Koenig M, et al. Among authors: lindlof m. Am J Hum Genet. 1989 Oct;45(4):498-506. Am J Hum Genet. 1989. PMID: 2491009 Free PMC article.
Carrier testing of children for two X-linked diseases: a retrospective evaluation of experience and satisfaction of subjects and their mothers.
Järvinen O, Lehesjoki AE, Lindlöf M, Uutela A, Kääriäinen H. Järvinen O, et al. Among authors: lindlof m. Genet Test. 1999;3(4):347-55. doi: 10.1089/gte.1999.3.347. Genet Test. 1999. PMID: 10627942
Carrier testing of children for two X-linked diseases: A retrospective study of comprehension of the test results and social and psychological significance of the testing.
Järvinen O, Lehesjoki AE, Lindlöf M, Uutela A, Kääriäinen H. Järvinen O, et al. Among authors: lindlof m. Pediatrics. 2000 Dec;106(6):1460-5. doi: 10.1542/peds.106.6.1460. Pediatrics. 2000. PMID: 11099604
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