Haltrich, Iren: search on Z-Library

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1

Jumping translocation of 17q11∼qter and 3q25∼q28 duplication in a variant Philadelphia t(9;14;22)(q34;q32;q11) in a childhood chronic myelogenous leukemia

Irén Haltrich, Maria Kost-Alimova, Gábor Kovács, Gergely Kriván, Júlia Tamáska, George Klein, György Fekete, Stefan Imreh

Journal:

Cancer Genetics and Cytogenetics

Year:

2006

Language:

english

File:

PDF, 509 KB

english, 2006

2

Multipoint interphase FISH in childhood T-acute lymphoblastic leukemia detects subpopulations that carry different chromosome 3 aberrations

Irén Haltrich, Maria Kost-Alimova, Gábor Kovács, Matild Dobos, George Klein, György Fekete, Stefan Imreh

Journal:

Cancer Genetics and Cytogenetics

Year:

2007

Language:

english

File:

PDF, 297 KB

english, 2007

3

Donor-cell myelodysplastic syndrome developing 13 years after marrow grafting for aplastic anemia

Irén Haltrich, Judit Müller, Judit Szabó, Gábor Kovács, Rozália Kóos, Anna Poros, Matild Dobos, György Fekete

Journal:

Cancer Genetics and Cytogenetics

Year:

2003

Language:

english

File:

PDF, 200 KB

english, 2003

4

Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients

Irén Haltrich, Maria Kost-Alimova, Gábor Kovács, George Klein, György Fekete, Stefan Imreh

Journal:

European Journal of Haematology

Year:

2006

Language:

english

File:

PDF, 631 KB

english, 2006

5

Gonadoblastoma: Case report of two young patients with isochromosome 12p found in the dysgerminoma overgrowth component in one case

Changchien, Yi-Che, Haltrich, Irén, Micsik, Tamás, Kiss, Eszter, Fónyad, László, Papp, Gergő, Sápi, Zoltán

Journal:

Pathology - Research and Practice

Year:

2012

Language:

english

File:

PDF, 840 KB

english, 2012

6

Six Cases of Rare Gene Amplifications and Multiple Copy of Fusion Gene in Childhood Acute Lymphoblastic Leukemia

Irén Haltrich, Monika Csóka, Gábor Kovács, Dóra Török, Donát Alpár, Gábor Ottoffy, György Fekete

Journal:

Pathology & Oncology Research

Year:

2013

Language:

english

File:

PDF, 273 KB

english, 2013

7

A de novo atypical ring sSMC(22) characterized by array CGH in a boy with cat-eye syndrome

Irén Haltrich,Henriett Pikó,Eszter Kiss,Zsuzsa Tóth…

Journal:

Molecular Cytogenetics

Year:

2014

Language:

english

File:

PDF, 714 KB

english, 2014

8

Enzymatic Regeneration of NAD in Enantioselective Oxidation of Secondary Alcohols: Glutamate Dehydrogenase Versus NADH Dehydrogenase

Lunzer, Regina, Ortner, Irene, Haltrich, Dietmar, Kulbe, Klaus D., Nidetzky, Bernd

Journal:

Biocatalysis and Biotransformation

Year:

1998

Language:

english

File:

PDF, 959 KB

english, 1998

9

Complex X chromosome rearrangement associated with multiorgan autoimmunity

Haltrich, Irén, Pikó, Henriett, Pamjav, Horolma, Somogyi, Anikó, Völgyi, Antónia, David, Dezső, Beke, Artúr, Garamvölgyi, Zoltán, Kiss, Eszter, Karcagi, Veronika, Fekete, György

Journal:

Molecular Cytogenetics

Year:

2015

Language:

english

File:

PDF, 2.58 MB

english, 2015

10

Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure

Beke, Artur, Piko, Henriett, Haltrich, Iren, Csomor, Judit, Matolcsy, Andras, Fekete, György, Rigo, Janos, Karcagi, Veronika

Journal:

Molecular Cytogenetics

Year:

2013

Language:

english

File:

PDF, 1.42 MB

english, 2013

11

Williams–Beuren-szindróma (Williams-szindróma)

Miklós, Györgyi, Fekete, György, Haltrich, Irén, Tóth, Miklós, Reismann, Péter

Journal:

Year:

2017

Language:

hungarian

File:

PDF, 744 KB

hungarian, 2017

12

A Transgenic Mouse Model for Detection of Tissue-Specific Thyroid Hormone Action

Mohácsik, Petra, Erdélyi, Ferenc, Baranyi, Mária, Botz, Bálint, Szabó, Gábor, Tóth, Mónika, Haltrich, Irén, Helyes, Zsuzsanna, Sperlágh, Beáta, Tóth, Zsuzsa, Sinkó, Richárd, Lechan, Ronald M, Bianco,

Journal:

Year:

2018

Language:

english

File:

PDF, 1.13 MB

english, 2018

13

Elsődleges genetikai vizsgálat Prader–Willi-szindróma igazolására

Ács, Orsolya Dóra, Péterfia, Bálint, Hollósi, Péter, Haltrich, Irén, Sallai, Ágnes, Luczay, Andrea, Buiting, Karin, Horsthemke, Bernhard, Török, Dóra, Szabó, András, Fekete, György

Journal:

Year:

2018

Language:

hungarian

File:

PDF, 405 KB

hungarian, 2018

14

Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations

Beke, Artur, Piko, Henriett, Haltrich, Iren, Karcagi, Veronika, Rigo, Janos, Molnar, Maria Judit, Fekete, György

Journal:

BMC Medical Genetics

Year:

2018

Language:

english

File:

PDF, 912 KB

english, 2018

15

Nemi kromoszóma-rendellenességek vizsgálata gyermekkorban

Pinti, Éva, Lengyel, Anna, Sallai, Ágnes, Fekete, György, Haltrich, Irén

Journal:

Year:

2018

Language:

hungarian

File:

PDF, 632 KB

hungarian, 2018

16

9p triszómia és a klinikai sokszínűség: egy váratlan megjelenésű eset ismertetése

Lengyel, Anna, Kosik, Anna, Pinti, Éva, Lódi, Csaba, Tory, Kálmán, Fekete, György, Haltrich, Irén

Journal:

Year:

2018

Language:

hungarian

File:

PDF, 1.16 MB

hungarian, 2018

17

Similar Cause, Different Phenotype: SOX9 Enhancer Duplication in a Family

Pinti, Eva, Piko, Henriett, Lengyel, Anna, Luczay, Andrea, Karcagi, Veronika, Fekete, Gyorgy, Haltrich, Iren

Journal:

Hormone Research in Paediatrics

Year:

2019

Language:

english

File:

PDF, 76 KB

english, 2019

18

Comprehensive profiling of disease-relevant copy number aberrations for advanced clinical diagnostics of pediatric acute lymphoblastic leukemia

Kiss, Richárd, Gángó, Ambrus, Benard-Slagter, Anne, Egyed, Bálint, Haltrich, Irén, Hegyi, Lajos, de Groot, Karel, Király, Péter Attila, Krizsán, Szilvia, Kajtár, Béla, Pikó, Henriett, Pajor, László, V

Journal:

Modern Pathology

Year:

2019

File:

PDF, 1.76 MB

2019

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