Publikationen von Reinhard Ullmann
Alle Typen
Zeitschriftenartikel (119)
101.
Zeitschriftenartikel
80 (2), S. 232 - 240 (2007)
Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius. American Journal of Human Genetics: AJHG / American Society of Human Genetics 102.
Zeitschriftenartikel
80 (2), S. 232 - 240 (2007)
Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius. American Journal of Human Genetics: AJHG / American Society of Human Genetics 103.
Zeitschriftenartikel
143 A (4), S. 333 - 337 (2007)
Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH. American Journal of Medical Genetics 104.
Zeitschriftenartikel
121 (3-4), S. 501 - 509 (2007)
Mutations in Autism Susceptibility Candidate 2 (AUTS2) in patients with mental retardation. Human Genetics 105.
Zeitschriftenartikel
67 (1), S. 408 - 416 (2007)
Allelic loss in a minimal region on chromosome 16q24 is associated with vitreous seeding of retinoblastoma. Cancer Research: an Official Organ of the American Association for Cancer Research 106.
Zeitschriftenartikel
14 (121), S. 1274 - 1279 (2006)
Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics. 107.
Zeitschriftenartikel
14 (121), S. 1274 - 1279 (2006)
Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics. 108.
Zeitschriftenartikel
115 (3-4), S. 247 - 253 (2006)
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research 109.
Zeitschriftenartikel
115 (3-4), S. 247 - 253 (2006)
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research 110.
Zeitschriftenartikel
70 (9), S. 1656 - 1660 (2006)
A complex phenotype with cystic renal disease. Kidney International: Official Journal of the International Society of Nephrology 111.
Zeitschriftenartikel
70 (9), S. 1656 - 1660 (2006)
A complex phenotype with cystic renal disease. Kidney International: Official Journal of the International Society of Nephrology 112.
Zeitschriftenartikel
115 (1), S. 84 - 89 (2006)
Characterisation of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development. Cytogenetics and Genome Research 113.
Zeitschriftenartikel
140A (8), S. 873 - 877 (2006)
A novel 8 Mb interstitial deletion of chromosome 8p12-p21.2. American Journal of Medical Genetics Part A 114.
Zeitschriftenartikel
118 (6), S. 708 - 715 (2006)
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly. Human Genetics 115.
Zeitschriftenartikel
6 (1), S. 1471 - 2105 (2005)
: CGHPRO – a comprehensive data analysis tool for array CGH. BMC Bioinformatics 116.
Zeitschriftenartikel
445 (2), S. 151 - 159 (2004)
Analysis of chromosome-11 aberrations in pulmonary and gastrointestinal carcinoids: an array comparative genomic hybridization-based study. Virchows Archiv: Official Journal of the European Society of Pathology 117.
Zeitschriftenartikel
203 (3), S. 798 - 807 (2004)
Protein expression profiles in adenocarcinomas and squamous cell carcinomas of the lung generated using tissue microarrays. Journal of Pathology: an Official Journal of the Pathological Society 118.
Zeitschriftenartikel
35 (5), S. 565 - 570 (2004)
Atypical goblet cell hyperplasia in congenital cystic adenomatoid malformation as a possible preneoplasia for pulmonary adenocarcinoma in childhood: A genetic analysis. Human Pathology 119.
Zeitschriftenartikel
39 (4), S. 263 - 276 (2004)
Distinct sequences on 11q13.5 and 11q23-24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients. Genes Chromosomes Cancer Buchkapitel (2)
120.
Buchkapitel
Array comparative genomic hybridization in pathology. In: Basic concepts of molecular pathology, S. 87 - 96 (Hg. Cagle, P. T.; Allen, T. C.). Springer, New York (2009)