Fluorescence in situ hybridization (FISH) : application guide / by Liehr, Thomas

Cytogenetic contribution to uniparental disomy (UPD) by Liehr Thomas

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FISH technology / by Rautenstrauss, Bernd W., 1959-, Liehr, Thomas, 1965-

Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl by Moassass Faten, Wafa Abdulsamad, Al Achkar Walid, Liehr Thomas

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A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3 by Mkrtchyan Hasmik, Wafa Abdulsamad, Al Achkar Walid, Moassass Faten, Liehr Thomas

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Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report by Moassass Faten, Mkrtchyan Hasmik, Wafa Abdulsamad, Al Achkar Walid, Liehr Thomas

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The hierarchically organized splitting of chromosomal bands for all human chromosomes by Liehr Thomas, Claussen Uwe, Mrasek Kristin, Weise Anja, Kosyakova Nadezda, Nelle Heike

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A new open access journal for a rapidly evolving biomedical field: introducing <it>Molecular Cytogenetics</it> by Yurov Yuri B, Liehr Thomas, Shaffer Lisa G, Iourov Ivan Y, Vorsanova Svetlana G

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Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them by Ogilvie Caroline, Kosyakova Nadezda, Mrasek Kristin, Liehr Thomas, Vermeesch Joris, Trifonov Vladimir, Rubtsov Nikolai

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Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon by Bhatt Samarth, Mrasek Kristin, Hunstig Friederike, Manvelyan Marina, Pellestor Franck, Weise Anja, Liehr Thomas

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Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics by Klein Elisabeth, Manvelyan Marina, Simonyan Isabella, Hamid Ahmed B, Guilherme Roberta, Liehr Thomas, Karamysheva Tatyana

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High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis) by Fan Xiaobo, Tanomtong Alongkoad, Chaveerach Arunrat, Pinthong Krit, Pornnarong Siripiyasing, Supiwong Weerayuth, Liehr Thomas, Weise Anja

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X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation by Melo Joana B, Almeida Joana, Liehr Thomas, Pinto Marta, Matoso Eunice, Ferreira Susana I, Carreira Isabel M

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Chromosome distribution in human sperm – a 3D multicolor banding-study by Mrasek Kristin, Bhatt Samarth, Hunstig Friederike, Manvelyan Marina, Pellestor Franck, Weise Anja, Simonyan Isabella, Aroutiounian Rouben, Liehr Thomas

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Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach... by Brečević Lukrecija, Rinčić Martina, Krsnik Željka, Sedmak Goran, Hamid Ahmed B., Kosyakova Nadezda, Galić Ivan, Liehr Thomas, Borovečki Fran

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Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report by Thieme Heike, von Eggeling Ferdinand, Mrasek Kristin, Alehan Dursun, Utine Eda, Weise Anja, Aktas Dilek, Tuncbilek Ergul, Liehr Thomas

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Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report by Hamid Ahmed B, Ewers Elisabeth, Plasencia Ana, Martínez-Frías María, Rodríguez Laura, Fernández-Toral Joaquín, Ziegler Monika, Liehr Thomas

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Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation by Brockmann Knut, Liehr Thomas, Boehm Detlef, Burfeind Peter, Zoll Barbara, Bruemmer Verena, Auber Bernd, Wilichowski Ekkehard, Argyriou Loukas, Bartels Iris

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Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder deli... by Neitzel Heidemarie, Sperling Karl, Tönnies Holger, Kosyakova Nadezda, Naumchik Irina, Rumyantseva Natalia, Khurs Olga, Polityko Anna, Weise Anja, Liehr Thomas

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Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report by Mulatinho Milene, de Carvalho Serao Cassio, Scalco Fernanda, Hardekopf David, Pekova Sona, Mrasek Kristin, Liehr Thomas, Weise Anja, Rao Nagesh, Llerena Juan

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