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UK Friedrich

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G Zafra de la Rosa; C A Venegas-Vega; Nancy Monroy; G Contreras-Bucio; UK Friedrich; M Houman; A Saad; P Fernández; Susana Kofman-Alfaro; Alicia Cervantes
Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.
UK Friedrich; M Houman; B H Hansen; Keld Kaltoft
Microdissection and reverse painting in a melanoma cell line: a detailed description of structurally abnormal chromosomes.
UK Friedrich; M Houman
[Microdissection of chromosomes].

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All Publications

2005: G Zafra de la Rosa; C A Venegas-Vega; Nancy Monroy; G Contreras-Bucio; UK Friedrich; M Houman; A Saad; P Fernández; Susana Kofman-Alfaro; Alicia Cervantes
Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.
American journal of medical genetics. Part A 2005;136(3):259-64.
2001: UK Friedrich; M Houman; B H Hansen; Keld Kaltoft
Microdissection and reverse painting in a melanoma cell line: a detailed description of structurally abnormal chromosomes.
Cancer genetics and cytogenetics 2001;125(1):5-9.
2000: UK Friedrich; M Houman
[Microdissection of chromosomes].
Ugeskrift for laeger 2000;162(45):6053-6.
2000: Merete Bugge; Gert Bruun-Petersen; Karen Brøndum-Nielsen; UK Friedrich; J Hansen; G Jensen; Peter Koch Jensen; Ulf Kristoffersson; Claes Lundsteen; Erik Niebuhr; K R Rasmussen; Kirsten Rasmussen; Niels Tommerup
Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.
Journal of medical genetics 2000;37(11):858-65.
2000: UK Friedrich; M Houman; J Sandgaard; A Rosgaard; Lone Sunde
Microdissection of chromosome 2--between-arm intrachromosomal insertion.
European journal of human genetics : EJHG 2000;8(5):393-5.
2000: UK Friedrich; Merete Bugge; M Houman; Karen Friis-Henriksen; Karen Brøndum-Nielsen
Microdissection - a precise method to disclose the parental origin of supernumerary marker chromosomes.
Annales de génétique 2000;43(2):109-10.
1997: Carsten A Brandt; H J Lüdecke; Johnny Hindkjaer; H Strømkjaer; D Pinkel; Troels Herlin; Lars Bolund; UK Friedrich
A de nevo complex t(7;13;8) translocation with a deletion in the TRPS gene region.
Human genetics 1997;100(3-4):334-8.
1997: Gabriele Senger; Ilse Chudoba; UK Friedrich; Niels Tommerup; Uwe Claussen; Karen Brøndum-Nielsen
Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
Prenatal diagnosis 1997;17(4):369-74.