Grimm T - Search Results

1

PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.

Decker E, Stellzig-Eisenhauer A, Fiebig BS, Rau C, Kress W, Saar K, Rüschendorf F, Hubner N, Grimm T, Weber BH. Decker E, et al. Among authors: grimm t. Am J Hum Genet. 2008 Dec;83(6):781-6. doi: 10.1016/j.ajhg.2008.11.006. Am J Hum Genet. 2008. PMID: 19061984 Free PMC article.

2

Primary failure of eruption (PFE)--clinical and molecular genetics analysis.

Stellzig-Eisenhauer A, Decker E, Meyer-Marcotty P, Rau C, Fiebig BS, Kress W, Saar K, Rüschendorf F, Hubner N, Grimm T, Witt E, Weber BH. Stellzig-Eisenhauer A, et al. Among authors: grimm t. J Orofac Orthop. 2010 Jan;71(1):6-16. doi: 10.1007/s00056-010-0908-9. Epub 2010 Feb 5. J Orofac Orthop. 2010. PMID: 20135246 English, German.

3

[Primary failure of eruption (PFE). Clinical and molecular genetics analysis].

Stellzig-Eisenhauer A, Decker E, Meyer-Marcotty P, Rau C, Fiebig BS, Kress W, Saar K, Rüschendorf F, Hubner N, Grimm T, Witt E, Weber BH. Stellzig-Eisenhauer A, et al. Among authors: grimm t. Orthod Fr. 2013 Sep;84(3):241-50. doi: 10.1051/orthodfr/2013055. Epub 2013 Sep 3. Orthod Fr. 2013. PMID: 23993365 French.

4

Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.

Grimm T, Kress W, Meng G, Müller CR. Grimm T, et al. Acta Myol. 2012 Dec;31(3):179-83. Acta Myol. 2012. PMID: 23620649 Free PMC article.

5

Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy.

Zirn B, Kress W, Grimm T, Berthold LD, Neubauer B, Kuchelmeister K, Müller U, Hahn A. Zirn B, et al. Among authors: grimm t. Am J Med Genet A. 2008 Apr 15;146A(8):1049-54. doi: 10.1002/ajmg.a.32259. Am J Med Genet A. 2008. PMID: 18348272

6

A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.

Rivera A, White K, Stöhr H, Steiner K, Hemmrich N, Grimm T, Jurklies B, Lorenz B, Scholl HP, Apfelstedt-Sylla E, Weber BH. Rivera A, et al. Among authors: grimm t. Am J Hum Genet. 2000 Oct;67(4):800-13. doi: 10.1086/303090. Epub 2000 Aug 24. Am J Hum Genet. 2000. PMID: 10958763 Free PMC article.

7

An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.

Kress W, Petersen B, Collmann H, Grimm T. Kress W, et al. Among authors: grimm t. Cytogenet Cell Genet. 2000;91(1-4):138-40. doi: 10.1159/000056834. Cytogenet Cell Genet. 2000. PMID: 11173846

8

Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.

Stec I, Kress W, Meng G, Müller B, Müller CR, Grimm T. Stec I, et al. Among authors: grimm t. J Med Genet. 1995 Dec;32(12):930-3. doi: 10.1136/jmg.32.12.930. J Med Genet. 1995. PMID: 8825917 Free PMC article.

9

X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysis.

Schuster V, Kress W, Friedrich W, Grimm T, Kreth HW. Schuster V, et al. Among authors: grimm t. Am J Dis Child. 1993 Dec;147(12):1303-5. doi: 10.1001/archpedi.1993.02160360045015. Am J Dis Child. 1993. PMID: 8249949

10

Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).

Kress W, Mueller-Myhsok B, Ricker K, Schneider C, Koch MC, Toyka KV, Mueller CR, Grimm T. Kress W, et al. Among authors: grimm t. Neuromuscul Disord. 2000 Oct;10(7):478-80. doi: 10.1016/s0960-8966(00)00129-2. Neuromuscul Disord. 2000. PMID: 10996776

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