Márta Czakó - ODT Personal data sheet

Publications

2021

Czakó Márta, Till Ágnes, Zima Judith, Zsigmond Anna, Szabó András, Maász Anita, Melegh Béla, Hadzsiev Kinga: Xp11.2 duplication in females: unique features of a rare copy number variation, FRONTIERS IN GENETICS 12: 635458
type of document: Journal paper/Article
number of independent citations: 2
language: English
URL

2019

Hadzsiev Kinga, Gyorsok Zsuzsanna, Till Agnes, Czakó Márta, Bartsch Oliver: Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect., CLINICAL DYSMORPHOLOGY 28: (3) pp. 137-141.
type of document:
number of independent citations: 5
language: English
URL

2019

Czakó Márta, Till Ágnes, Szabó András, Ripszám Réka, Melegh Béla, Hadzsiev Kinga: Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 20: (19) 4935
type of document: Journal paper/Article
language: English
URL

2018

Szabo A, Czako M, Hadzsiev K, Duga B, Banfai Z, Komlosi K, Melegh B: Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene, AMERICAN JOURNAL OF MEDICAL GENETICS PART A 176: (2) pp. 443-449.
type of document: Journal paper/Article
number of independent citations: 7
language: English
URL

2016

Hadzsiev K, Komlosi K, Czako M, Duga B, Szalai R, Szabo A, Postyeni E, Szabo T, Kosztolanyi G, Melegh B: Kleefstra syndrome in Hungarian patients: additional symptoms besides the classic phenotype., MOLECULAR CYTOGENETICS 9: 22
type of document:
number of independent citations: 13
language: English
URL

2015

Komlosi K, Duga B, Hadzsiev K, Czako M, Kosztolanyi G, Fogarasi A, Melegh B: Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome., MOLECULAR CYTOGENETICS 8: 16
type of document: Journal paper/Article
number of independent citations: 10
language: English
URL

2012

Czako M, Hadzsiev K, Melegh B, Kosztolanyi G: Jumping translocation of 15q24-qter resulting in partial trisomy: A case report, GENE 503: (1) pp. 155-159.
type of document: Journal paper/Article
number of independent citations: 3
language: English
URL

2005

Kellermayer R, Gyarmati J, Czakó M, Tészás A, Masszi GY, Ertl T, Kosztolányi GY: Mos 46,XX,r(18).ish r(18)(18ptel-,18qtel-)/46,XX.ish del(18)(18ptel-): an example for successive ring chromosome formation., AMERICAN JOURNAL OF MEDICAL GENETICS PART A 139A: (3) pp. 234-235.
type of document:
number of independent citations: 3
language: English
URL

2004

Czakó M, Riegel M, Morava É, Bajnóczky K, Kosztolányi GY: Opitz "C" trigonocephaly-like syndrome in a patient with terminal deletion of 2p and partial duplication of 17q, AMERICAN JOURNAL OF MEDICAL GENETICS PART A 131A: (3) pp. 310-312.
type of document: Journal paper/Article
number of independent citations: 16
language: English
URL

2002

Czakó M, Riegel M, Morava É, Schinzel A, Kosztolányi GY: Patient with rheumatoid arthritis and MCA/MR syndrome due to unbalance der(18) transmission of a paternal translocation t(18;20)(p11.1;p11.1), AMERICAN JOURNAL OF MEDICAL GENETICS 108: pp. 226-228.
type of document: Journal paper/Article
number of independent citations: 9
language: English
URL

Number of independent citations to these publications: