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Anais Brasileiros de Dermatologia, ISSN 0365-0596, 07/2013, Volume 88, Issue 4, pp. 507 - 517
Journal Article
Brazilian Journal of Biology, ISSN 1519-6984, 11/2004, Volume 64, Issue 5, pp. 885 - 890
Somatic recombination in heterozygous diploid cells may be a promotional agent of neoplasms by inducing homozygosity of defective genes. Tumor suppressor genes... 
índice de homozigotização | loss of heterozygozity | mitotic crossing-over | crossing-over mitótico | homozygotization index | Ricinus communis | perda de heterozigozidade
Journal Article
Medizinische Genetik, ISSN 0936-5931, 12/2010, Volume 22, Issue 4, pp. 429 - 433
Journal Article
Der Pathologe, ISSN 0172-8113, 11/2011, Volume 32, Issue S2, pp. 197 - 201
Adenokarzinome im distalen Ösophagus entstehen mehrheitlich aus einer intestinalen Metaplasie (Barrett-Ösophagus) über die Zwischenstufen einer niedrig- und... 
Adenocarcinoma | Immunohistochemistry | Pathology | Immunhistochemie | Medicine & Public Health | Tumor markers, biological | Risikobewertung | Risk assessment | Tumormarker, biologische | Loss of heterozygosity | Adenokarzinome
Journal Article
Medizinische Genetik, ISSN 0936-5931, 12/2010, Volume 22, Issue 4, pp. 434 - 438
Journal Article
medizinische genetik, ISSN 0936-5931, 6/2012, Volume 24, Issue 2, pp. 114 - 122
Array-basierte Methoden zum Nachweis chromsomaler Imbalancen haben in der vergangenen Dekade zunehmende Bedeutung in der tumorgenetischen Analytik gewonnen.... 
Human Genetics | Pediatrics | Einzelnukleotidpolymorphismus | Cancer genetics | Chromosomal imbalances | Verlust der Heterozygotie | Chromosomale Imabalancen | Array comparative genomic hybridization | Tumorgenetik | Biomedicine | Obstetrics/Perinatology | Loss of heterozygosity | Single nucleotide polymorphism | Reproductive Medicine
Journal Article
medizinische genetik, ISSN 0936-5931, 12/2010, Volume 22, Issue 4, pp. 429 - 433
Mutationen beider Allele des Retinoblastomgens (RB1) sind Voraussetzung für die Entstehung des Retinoblastoms. Dieser Augentumor kann auf der Grundlage einer... 
Human Genetics | Pediatrics | Genetische Prädisposition | Genetisches Imprinting | Genetic predisposition | Allele | Biomedicine | Retinoblastoma genes | Retinoblastomgene | Obstetrics/Perinatology | Loss of heterozygosity | Alleles | Genetic imprinting | Reproductive Medicine
Journal Article
medizinische genetik, ISSN 0936-5931, 12/2010, Volume 22, Issue 4, pp. 434 - 438
Hereditäre Paragangliome/Phäochromozytome werden autosomal-dominant vererbt. Es lassen sich 3 Formen, PGL1, PGL3 und PGL4 unterscheiden. Sie werden verursacht... 
Human Genetics | Pediatrics | Komplex II der mitochondrialen Atmungskette | Pheochromocytoma | Electron transport complex II | Paraganglioma | Multiple endocrine neoplasia type 2 | Phäochromozytom | Biomedicine | Obstetrics/Perinatology | Loss of heterozygosity | Paragangliom | Multiple endokrine Neoplasie 2 | Reproductive Medicine
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 09/2006, Volume 81, Issue 5, pp. 405 - 419
Journal Article
European Urology, ISSN 0302-2838, 2017, Volume 72, Issue 1, pp. 34 - 42
Journal Article
Journal Article
International Journal of Cancer, ISSN 0020-7136, 03/2017, Volume 140, Issue 6, pp. 1364 - 1369
Journal Article
Neurocirugía, ISSN 1130-1473, 2007, Volume 18, Issue 4, pp. 285 - 293
Analizar en tumores cerebrales, fundamentalmente de estirpe neuro-epitelial, la existencia de mutaciones en los cromosomas 1p y 19q por la técnica de análisis... 
Cerebral tumors | 1p/19q mutation | Mutación 1p/19q | Gliomas | Loss of heterozygosity | Tumores cerebrales | Alquilantes | Alkylating drugs | Pérdida de heterocigocidad | 19q | Mutación 1p
Journal Article