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A genome-wide search for linkage to asthma. German Asthma Genetics Group.
Genomics. 1999 May 15;58(1):1-8. doi: 10.1006/geno.1999.5806.
Genomics. 1999.
PMID: 10333435
Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity.
Saar K, Al-Gazali L, Sztriha L, Rueschendorf F, Nur-E-Kamal M, Reis A, Bayoumi R.
Saar K, et al. Among authors: rueschendorf f.
Am J Hum Genet. 1999 Dec;65(6):1666-71. doi: 10.1086/302655.
Am J Hum Genet. 1999.
PMID: 10577920
Free PMC article.
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A novel form of "central pouchlike" cataract, with sutural opacities, maps to chromosome 15q21-22.
Vanita, Singh JR, Sarhadi VK, Singh D, Reis A, Rueschendorf F, Becker-Follmann J, Jung M, Sperling K.
Vanita, et al. Among authors: rueschendorf f.
Am J Hum Genet. 2001 Feb;68(2):509-14. doi: 10.1086/318189. Epub 2000 Dec 21.
Am J Hum Genet. 2001.
PMID: 11133359
Free PMC article.
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Clinical and genetic features in a family with CADASIL and high lipoprotein (a) values.
Gong M, Rueschendorf F, Marx P, Schulz H, Kraft HG, Huebner N, Koennecke HC.
Gong M, et al. Among authors: rueschendorf f.
J Neurol. 2010 Aug;257(8):1240-5. doi: 10.1007/s00415-010-5496-5. Epub 2010 Feb 9.
J Neurol. 2010.
PMID: 20143106
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