E-LIB Suche - Ergebnisse für: Koczok, Katalin

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#1558 Mutational spectrum of X-linked hypophosphatemia (XLH..:

Balogh, Istvan ; Szabo, Tamas ; Reusz, Gyorgy...
Nephrology Dialysis Transplantation. 39 (2024) Supplement_1 - p. , 2024

Link: https://doi.org/10.1093/..

2

Genetic counselling legislation and practice in cancer in E..:

McCrary, J Matt ; Van Valckenborgh, Els ; Poirel, Hélène A...
European Journal of Public Health. , 2024

Link: https://doi.org/10.1093/..

3

Double Heterozygosity for Rare Deleterious Variants in the ..:

Madar, László ; Majoros, Viktória ; Szűcs, Zsuzsanna...
International Journal of Molecular Sciences. 24 (2023) 20 - p. 15334 , 2023

Link: https://doi.org/10.3390/..

4

Double Heterozygosity for Rare Deleterious Variants in the ..:

László Madar ; Viktória Majoros ; Zsuzsanna Szűcs...
https://www.mdpi.com/1422-0067/24/20/15334. , 2023

Link: https://doi.org/10.3390/..

5

Double Heterozygosity for Rare Deleterious Variants in the ..:

Madar, László ; Majoros, Viktória ; Szűcs, Zsuzsanna...
International Journal Of Molecular Sciences. -24 : 20 (2023), p. 1-7. -Int. J. Mol. Sci. - 1422-0067. , 2023

Link: https://hdl.handle.net/2..

6

Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectoderm..:

Szabó, Tímea Margit ; Balogh, István ; Ujfalusi, Anikó...
Genes. 13 (2022) 12 - p. 2367 , 2022

Link: https://doi.org/10.3390/..

7

An Ultra-Rare Manifestation of an X-Linked Recessive Disord..:

Szűcs, Zsuzsanna ; Pinti, Éva ; Haltrich, Irén...
International Journal of Molecular Sciences. 23 (2022) 21 - p. 13076 , 2022

Link: https://doi.org/10.3390/..

8

A magyar Cystás Fibrosis Regiszter genetikai revíziója:

Deák, Anna ; Koczok, Katalin ; Bessenyei, Beáta...
Orvosi Hetilap. 163 (2022) 51 - p. 2052-2059 , 2022

Link: https://doi.org/10.1556/..

9

Cytogenetic Investigation of Infertile Patients in Hungary:..:

Andó, Szilvia ; Koczok, Katalin ; Bessenyei, Beáta..
Genes. 13 (2022) 11 - p. 2086 , 2022

Link: https://doi.org/10.3390/..

10

Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectoderm..:

Tímea Margit Szabó ; István Balogh ; Anikó Ujfalusi...
https://www.mdpi.com/2073-4425/13/12/2367. , 2022

Link: https://doi.org/10.3390/..

11

An Ultra-Rare Manifestation of an X-Linked Recessive Disord..:

Zsuzsanna Szűcs ; Éva Pinti ; Irén Haltrich...
Molecular Pathology, Diagnostics, and Therapeutics. , 2022

Link: https://doi.org/10.3390/..

12

Helsmoortel-Van der Aa Syndrome: Cardiothoracic and Ectoder..:

Szabó, Tímea Margit ; Balogh, István ; Ujfalusi, Anikó...
Genes. -13 : 12 (2022), p. 1-13. -Genes. - 2073-4425. , 2022

Link: https://hdl.handle.net/2..

13

An Ultra-Rare Manifestation of an X-Linked Recessive Disord..:

Szűcs, Zsuzsanna ; Pinti, Éva ; Haltrich, Irén...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655586/. , 2022

Link: http://www.ncbi.nlm.nih...

14

An Ultra-Rare Manifestation of an X-Linked Recessive Disord..:

Zsuzsanna Szűcs ; Éva Pinti ; Irén Haltrich...
https://www.mdpi.com/1422-0067/23/21/13076. , 2022

Link: https://doi.org/10.3390/..

15

Cytogenetic Investigation of Infertile Patients in Hungary:..:

Andó, Szilvia ; Koczok, Katalin ; Bessenyei, Beáta..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9690888/. , 2022

Link: http://www.ncbi.nlm.nih...