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Featured researches published by Ivan Balazs.


Human Genetics | 1984

Isolation and subregional mapping of a human cDNA clone detecting a common RELP on chromosome 12

Ivan Balazs; Michele Purrello; Becky Alhadeff; K.-H. Grezeschik; Paul Szabo

SummarycDNA libraries are a potential source of DNA probes which can be used to screen for restriction fragment length polymorphisms (RFLPs). This approach had not been exploited until recently; in this and another paper (Balazs et al. 1984) we show that they can be a fruitful source for such probes. As an example herein we describe a common EcoRI polymorphism, detected by a randomly selected cDNA probe of unknown function. This sequence has been mapped to human chromosome 12, band q21, through the combined use of somatic cell genetics, DNA recombinant technology, and in situ hybridization.


Somatic Cell and Molecular Genetics | 1978

Hybridization properties of human X-chromosomal RNA transcripts from murine-human hybrids

Ivan Balazs; P. Szabo; Marcello Siniscalco

A human-mouse hybrid cell line which has retained the human X chromosome and a fragment of chromosome 2 contains RNA sequences transcribed from human DNA. Nuclear RNA enriched for human sequences was prepared from this hybrid cell line by a multistep hybridization procedure to mouse and human DNA immobilized on nitrocellulose filters. The properties of this RNA were analyzed by RNA-DNA hybridization techniques. The results indicate that we have pre pared a RNA fraction enriched for sequences homologous to repeated DNA sequences of the human X chromosome.


American Journal of Medical Genetics | 1983

Brief report: Linkage between G6PD and fragile‐X syndrome

Giorgio Filippi; Antoniettina Rinaldi; Nicoletta Archidiacono; Mariano Rocchi; Ivan Balazs; Marcello Siniscalco


Archive | 1994

Molecular genetic identification using probes that recognize polymorphic loci

Ivan Balazs; Zvi G. Loewy; John Neuweiler; Howard J. Baum; Vivian Ruvolo


American Journal of Medical Genetics | 1990

DNA linkage analysis and studies of the androgen receptor gene in a large kindred with complete androgen insensitivity

Julianne Imperato-McGinley; Nancy Y. Ip; Teofilo Gautier; John Neuweiler; Harry Gruenspan; Shutsung Liao; Chawnshang Chang; Ivan Balazs


Proceedings of the National Academy of Sciences of the United States of America | 1982

Highly polymorphic DNA site D14S1 maps to the region of Burkitt lymphoma translocation and is closely linked to the heavy chain γ1 immunoglobulin locus

Ivan Balazs; Michele Purrello; Pablo Rubinstein; Becky Alhadeff; Marcello Siniscalco


American Journal of Medical Genetics | 1995

X‐linked ichthyosis without STS deficiency: Clinical, genetical, and molecular studies

Renato Robledo; Paola Melis; Erika Schillinger; Ida Casciano; Ivan Balazs; Antoniettina Rinaldi; Marcello Siniscalco; Giorgio Filippi


Nucleic Acids Research | 1990

Isolation and characterization of a hypervariable region [D4S163] on chromosome 4

John Neuweiler; Vivian Ruvolo; Howard J. Baum; Karl-Heinz Grzeschik; Ivan Balazs


Nucleic Acids Research | 1989

Discovery of a novel multilocus DNA polymorphism [DNF24]

Nancy Y. Ip; Leric Nicholas; Howard J. Baum; Ivan Balazs


Nucleic Acids Research | 1989

Identification and characterization of a hypervariable region [D18S27] on chromosome 18

Nancy Y. Ip; I. van de Stadt; Zvi G. Loewy; Susan L. Leary; Karl-Heinz Grzeschik; Ivan Balazs

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Nancy Y. Ip

Hong Kong University of Science and Technology

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P. Szabo

Kettering University

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Chawnshang Chang

University of Rochester Medical Center

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