Haaf T - Search Results

1

D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection.

Lemmers RJ, Osborn M, Haaf T, Rogers M, Frants RR, Padberg GW, Cooper DN, van der Maarel SM, Upadhyaya M. Lemmers RJ, et al. Among authors: haaf t. Neurology. 2003 Jul 22;61(2):178-83. doi: 10.1212/01.wnl.0000078889.51444.81. Neurology. 2003. PMID: 12874395

2

Complex FISH probes for the subtelomeric regions of all human chromosomes: comparative hybridization of CEPH YACs to chromosomes of the Old World monkey Presbytis cristata and great apes.

Kingsley K, Wirth J, van der Maarel S, Freier S, Ropers HH, Haaf T. Kingsley K, et al. Among authors: haaf t. Cytogenet Cell Genet. 1997;78(1):12-9. doi: 10.1159/000134616. Cytogenet Cell Genet. 1997. PMID: 9345897

3

Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes.

Wirth J, Nothwang HG, van der Maarel S, Menzel C, Borck G, Lopez-Pajares I, Brøndum-Nielsen K, Tommerup N, Bugge M, Ropers HH, Haaf T. Wirth J, et al. Among authors: haaf t. J Med Genet. 1999 Apr;36(4):271-8. J Med Genet. 1999. PMID: 10227392 Free PMC article.

4

Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?

Stout K, van der Maarel S, Frants RR, Padberg GW, Ropers HH, Haaf T. Stout K, et al. Among authors: haaf t. Chromosome Res. 1999;7(5):323-9. doi: 10.1023/a:1009287111661. Chromosome Res. 1999. PMID: 10515207

5

A cascade of complex subtelomeric duplications during the evolution of the hominoid and Old World monkey genomes.

van Geel M, Eichler EE, Beck AF, Shan Z, Haaf T, van der Maarel SM, Frants RR, de Jong PJ. van Geel M, et al. Among authors: haaf t. Am J Hum Genet. 2002 Jan;70(1):269-78. doi: 10.1086/338307. Epub 2001 Nov 30. Am J Hum Genet. 2002. PMID: 11731935 Free PMC article.

6

Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2.

Haaf T, Willard HF. Haaf T, et al. Genomics. 1992 May;13(1):122-8. doi: 10.1016/0888-7543(92)90211-a. Genomics. 1992. PMID: 1577477

7

Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations.

Nothwang HG, Schröer A, van der Maarel S, Kübart S, Schneider S, Riesselmann L, Menzel C, Hinzmann B, Vogt D, Rosenthal A, Fryns J, Tommerup N, Haaf T, Ropers HH, Wirth J. Nothwang HG, et al. Among authors: haaf t. Cytogenet Cell Genet. 2000;90(1-2):126-33. doi: 10.1159/000015647. Cytogenet Cell Genet. 2000. PMID: 11060462

8

Centromeric association of chromosome 16- and 18-derived microchromosomes.

Felbor U, Rutschow D, Haaf T, Schmid M. Felbor U, et al. Among authors: haaf t. Hum Genet. 2002 Jul;111(1):16-25. doi: 10.1007/s00439-002-0744-0. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136231

9

Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein-Taybi syndrome.

Bartsch O, Rasi S, Delicado A, Dyack S, Neumann LM, Seemanová E, Volleth M, Haaf T, Kalscheuer VM. Bartsch O, et al. Among authors: haaf t. Hum Genet. 2006 Sep;120(2):179-86. doi: 10.1007/s00439-006-0215-0. Epub 2006 Jun 17. Hum Genet. 2006. PMID: 16783566

10

Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

Vona B, Nanda I, Neuner C, Schröder J, Kalscheuer VM, Shehata-Dieler W, Haaf T. Vona B, et al. Among authors: haaf t. BMC Med Genet. 2014 Jun 25;15:72. doi: 10.1186/1471-2350-15-72. BMC Med Genet. 2014. PMID: 24962056 Free PMC article. Review.

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