Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding

by Weise Anja, Mrasek Kristin, Karadeniz Nilüfer
Published 2008-08-01

The hierarchically organized splitting of chromosomal bands for all human chromosomes

by Liehr Thomas, Claussen Uwe, Mrasek Kristin, Weise Anja, Kosyakova Nadezda, Nelle Heike
Published 2009-01-01

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
Published 2008-04-01

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
Published 2014-01-01

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
Published 2008-11-01

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
Published 2009-06-01

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
Published 2010-03-01

Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boy

by Oliveira Guiomar, Kosyakova Nadezda, Weise Anja, Vermeesch Joris, Backx Liesbeth, Rodrigues Carlos, Melo Joana B, Carreira Isabel M, Matoso Eunice
Published 2009-08-01

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
Published 2012-06-01

Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-...

by Kokotas Haris, Orru Sandro, Mihalatos Markos, Weise Anja, Neroutsou Rozita, Thomaidis Loreta, Kosyakova Nadezda, Manolakos Emmanouil, Kitsos George, Liehr Thomas, Petersen Michael B
Published 2008-11-01

A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report

by Vermeesch Joris, Andrieux Joris, Desai Manisha, Sheth Jayesh, Weise Anja, Kosyakova Nadezda, Ewers Elisabeth, Sheth Frenny, Hamid Ahmed B, Ziegler Monika, Liehr Thomas
Published 2009-11-01

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

by Garas Antonios, Weise Anja, Ewers Elisabeth, Kosyakova Nadezda, Kontodiou Maria, Lagou Magdalini, Manolakos Emmanouil, Kitsiou-Tzeli Sofia, Orru Sandro, Liehr Thomas, Metaxotou Aikaterini
Published 2009-01-01

Derivative chromosome 1 and <it>GLUT1 </it>deficiency syndrome in a sibling pair

by Akarsu Nurten, Posorski Nicole, Yalaz Kalbiye, von Eggeling Ferdinand, Weise Anja, Mrasek Kristin, Utine Eda G, Aktas Dilek, Alikasifoglu Mehmet, Liehr Thomas, Tuncbilek Ergul
Published 2010-05-01

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

by Garas Antonios, Weise Anja, Ewers Elisabeth, Kosyakova Nadezda, Kontodiou Maria, Anagnostopoulou Katerina, Lagou Magdalini, Manolakos Emmanouil, Kitsiou-Tzeli Sofia, Orru Sandro, Liehr Thomas, Metaxotou Aikaterini
Published 2009-02-01

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

by Mkrtchyan Hasmik, Kosyakova Nadezda, Gross Madeleine, Rodriguez Laura, Anderson Jasen, Nandini Adayapalam, Binkert Franz, Fluri Simon, Trifonov Vladimir, Ewers Elisabeth, Reich Daniela, Weise Anja, Liehr Thomas
Published 2008-04-01

Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literatur...

by Kolotii Alexei D, Monakhov Victor V, Weise Anja, Voinova-Ulas Victoria Y, Iourov Ivan Y, Vorsanova Svetlana G, Soloviev Ilia V, Novikov Petr V, Yurov Yuri B, Liehr Thomas
Published 2008-06-01

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
Published 2012