ESTEFANIA LANDI; LILIANA KARABATAS; TOMAS RODRIGUEZ GOMEZ; PAULA SCAGLIA; LAURA RAMIREZ; ANA KESELMAN; DEBORA BRASLAVSKY; NORA SANGUINETTI; PATRICIA PENNISI; RODOLFO REY; IGNACIO BERGADA; HECTOR JASPER; HORACIO DOMENE; PAOLA PLAZAS; SABINA DOMENE

An in vivo functional assay to characterize human STAT5B genetic variants during zebrafish development

International Meeting Pediatric Endocrinology

Lugar: Buenos Aires; Año: 2023;

SANGUINETI, NORA; SCAGLIA, PAULA; KESELMAN, ANA; CASALI, BÁRBARA; BRASLAVSKY, DEBORA; GUTIERREZ, MARIANA; LAURA RAMIREZ; LANDI, ESTEFANÍA; ROPELATO, MARIA GABRIELA; BALLERINI, MARIA GABRIELA; PENNISI, PATRICIA; MARTIN, AYELEN; VAZQUEZ, MARTIN; CASSINELLI, HAMILTON; DOMENE, SABINA; ARIEL BERENSTEIN; IZQUIERDO, AGUSTIN; DEL REY, GRACIELA; VILLEGAS, F; ARMANDO, ROMINA; AZCOITI, MARÍA ESNAOLA; ARBERAS, CLAUDIA; DOMENE, HORACIO; JASPER, HECTOR; ARNHOLD, I; VASQUES, GABRIELA; JORGE, ALEXANDER; REY, RODOLFO; BERGADA, IGNACIO

Potentially pathogenic variants identified by next generation sequencing in patients with short stature of unknown origin.

Sociedad Latinoamericana de Endocrinologia Pediatrica

Lugar: Merida; Año: 2020;

LANDI, ESTEFANÍA; KARABATAS, LILIANA; LAURA RAMIREZ; GUTIERREZ, MARIANA; SCAGLIA, PAULA; KESELMAN, ANA; BRASLAVSKY, DEBORA; SANGUINETI, NORA; BERGADA, IGNACIO; JASPER, HECTOR; DOMENE, HORACIO; PLAZAS, PAOLA VIVIANA; DOMENE, SABINA

A Novel Human Heterozygous STAT5B Variant Leads to Impaired Growth and Developmental Defects in Zebrafish Embryos

Annual Meeting of the Endocrine Society

Lugar: San Francisco; Año: 2020;

ESTEFANIA LANDI; LILIANA KARABATAS; LAURA RAMIREZ; MARIANA GUTIERREZ; PAULA SCAGLIA; ANA KESELMAN; DEBORA BRASLAVSKY; NORA SANGUINETTI; IGNACIO BERGADA; HECTOR JASPER; HORACIO DOMENE; PLAZAS, PAOLA VIVIANA; DOMENE, SABINA

A novel human heterozygous STAT5B variant leads to growth and developmental defects in zebrafish embryos

Sociedad Argentina de Investigaciones Clínicas (SAIC)

Año: 2019;

NORA MARÍA SANGUINETI; LAURA RAMIREZ; ANA CLAUDIA KESELMAN; PAULA SCAGLIA; MARIA GABRIELA ROPELATO; MARIA GABRIELA BALLERINI; LILIANA KARABATAS; SABINA DOMENE; LUCIA MARTUCCI; DEBORA BRASLAVSKY; ESTEFANIA LANDI; HAMISLTON CASSINELLI; BARBARA CASALI; GRACIELA DEL REY; PATRICIA PENNISI; HECTOR JASPER; MARTIN VAZQUEZ; RODOLFO REY; HORACIO DOMENE; MARIANA GUTIERREZ; IGNACIO BERGADA

Monogenic and Digenic Gene Mutations Are Present in Children with Idiopathic Short Stature (ISS)

European Society for Paediatric Endocrinology (ESPE)

Año: 2018;

LAURA RAMIREZ; NORA SANGUINETTI; ANA KESELMAN; PAULA SCAGLIA; ARIEL BERENSTEIN; MARIA GABRIELA ROPELATO; MARIA GABRIELA BALLERINI; LILIANA KARABATAS; SABINA DOMENE; LUCIA MARTUCCI; DEBORA BRASLAVSKY; HAMILTON CASSINELLI; BARBARA CASALI; GRACIELA DEL REY; PATRICIA PENNISI; HECTOR JASPER; MARTIN VAZQUEZ; RODOLFO REY; HORACIO DOMENE; IGNACIO BERGADA; MARIANA GUTIERREZ

Short Stature Associated to Partial Growth Hormone Insensitivity (GHI) Due to a Digenic Disorder with a Hypomorphic Variant in IGFALS Combined to a Novel Heterozygous STAT5B Missense Variant

Congreso Latinoamericano de Endocrinología pediátrica (SLEP)

Año: 2018;

ESTEFANIA LANDI; PAOLA PLAZAS; PAULA SCAGLIA; LUCIA MARTUCCI; HECTOR JASPER; HORACIO DOMENE; SABINA DOMENE

An in vivo zebrafish functional assay to characterize IGFALS gene variants

Reunion conjunta de sociedades de biociencias

Lugar: Buenos Aires; Año: 2017;

CASTAGNOLA TAIS; DOMENE, SABINA; CARPANETO AGUSTIN; SALATINO LUCIA; ELGOYHEN ANA BELEN; PLAZAS PAOLA

Analysis of the expression patterns of zebrafish nicotinic acetylcholine receptor subunits at the efferent-lateral line synapse

Sociedad Argentina de Investigacion en Neurociencias

Lugar: Mar del plata; Año: 2017;

CASTAGNOLA TAIS; DOMENE SABINA; CARPANETO AGUSTIN; SALATINO LUCIA; DALAMON VIVIANA; ELGOYHEN ANA BELEN; PLAZAS PAOLA

Spatiotemporal expression of zebrafish nicotinic acetylcholine receptor at the efferent-lateral line synapse

Federation of Latin American and Caribean Neuroscience

Lugar: Buenos Aires; Año: 2016;

GUTIERREZ, MARIANA; SCAGLIA, PAULA; KESELMAN, ANA; MARTUCCI, LUCIA; KARABATAS, LILIANA; DOMENÉ SABINA; BLANCO, MIGUEL; SANGUINETTI, NORA; BEZRODNIK, LILIANA; DI GIOVANNI, DANIELA; CALDIROLA, MARIA SOLEDAD; ESNAOLA AZCOITI, M; HAWA-JONES, N; HWA, VIVIAN; REVALE, SANTIAGO; VAZQUEZ, MARTIN; JASPER, HECTOR; KUMAR, ASHISH; DOMENE, HORACIO

Functional In Vitro Characterization of Two Novel Germinal STAT3 Mutations Associated with Short Stature, Immunedeficiency and Autoimmune Disease

European Society for Pediatric Endocrinology (ESPE)

Lugar: Paris; Año: 2016;

SCAGLIA, PAULA; KESELMAN, ANA; BRASLAVSKY, DEBORA; MARTUCCI, LUCIA; KARABATAS, LILIANA; DOMENE SABINA; GUTIERREZ, MARIANA; BALLERINI, MARIA GABRIELA; ROPELATO, MARIA GABRIELA; SPINOLA-CASTRO, ANGELA MARIA; SIVIERO-MIACHON, A; SAITO TARTUCI, J; RODRIGUEZ AZRAK, SOL; REY, RODOLFO; JASPER, HECTOR; BERGADA, IGNACIO; DOMENE, HORACIO

Characterization of Four Latin-American Families Confirms Previous Findings and Reveals Novel Features of ALS Deficiency.

Sociedad Latinoamericana de Endocrinologia Pediatrica

Lugar: Buenos Aires; Año: 2016;

GUTIERREZ, MARIANA; SCAGLIA, PAULA; MARTUCCI, LUCIA; KARABATAS, LILIANA; DOMENE, SABINA; BLANCO, MIGUEL; SANGUINETTI, NORA; BEZRODNIK, LILIANA; DI GIOVANNI, DANIELA; CALDIROLA, MARIA SOLEDAD; ESNAOLA AZCOITI, M; JONES, N; HWA, VIVIAN; REVALE, SANTIAGO; VAZQUEZ, MARTIN; JASPER, HECTOR; KUMAR, ASHISH; DOMENE, HORACIO

In Vitro Characterization Of Two STAT3 Gain Of Function Mutations Associated With IGF-1 Deficiency And Immune Dysregulation.

Sociedad Latinoamericana de Endocrinologia Pediatrica (SLEP)

Lugar: Buenos Aires; Año: 2016;

KESELMAN, ANA; BRASLAVSKY, DEBORA; SCAGLIA, PAULA; KARABATAS, LILIANA; BALLERINI, MARIA GABRIELA; MARTUCCI, LUCIA; GUTIERREZ, MARIANA; DOMENÉ SABINA; MARTINEZ, ALICIA; ROPELATO, MARIA GABRIELA; BERGADA, IGNACIO; DOMENE, HORACIO; JASPER, HECTOR

Clinical and Biochemical Response to rhGH Treatment in Children with Idiopathic Short Stature (ISS): Impact of Heterozygous Variants in the IGFALS Gene.

Sociedad Latinoamericana de Endocrinologia Pediatrica (SLEP)

Lugar: Buenos Aires; Año: 2016;

MARTUCCI, LUCIA; SCAGLIA, PAULA; GUTIERREZ, MARIANA; KARABATAS, LILIANA; REY, RODOLFO; DOMENE, HORACIO; DOMENE, SABINA; JASPER, HECTOR

Estudio de la expresión in vitro de variantes del gen IGFALS halladas en niños con deficiencia de ALS (ALS-D) o con talla baja idiopática (TBI)

Sociedad Argentina de Investigacion Clinica (SAIC)

Lugar: Mar del Plata; Año: 2015;

SCAGLIA, PAULA; BERGADA, IGNACIO; BRASLAVSKY, DEBORA; KESELMAN, ANA; CASTRO, ANGELA ESPINOSA; DOMENÉ SABINA; JASPER, HECTOR; DOMENE, HORACIO

Gene founder effect: The underlying mechanism of recurrent IGFALS mutations

Sociedad Latinoamericana de Endocrinologia Pediatrica

Lugar: Puerto Varas; Año: 2015;

SCAGLIA, PAULA; SALA, ANDREA; BERGADA, IGNACIO; BRASLAVSKY, DEBORA; KESELMAN, ANA; CASTRO, ANGELA ESPINOSA; DOMENE, SABINA; JASPER, HECTOR; CORACH, DANIEL; DOMENE, HORACIO

Recurrent IGFALS gene mutations p.E35Gfs*17 and p.[L409F;A475V]: hot spot or founder effect?

European Society of Pediatric Endocrinology

Lugar: Barcelona; Año: 2015;

SCAGLIA, PAULA; KESELMAN, ANA; GUTIERREZ, MARIANA; DOMENÉ SABINA; BLANCO, MIGUEL; SANGUINETTI, NORA; BEZRODNIK, LILIANA; DI GIOVANNI, DANIELA; CALDIROLA, MARIA SOLEDAD; MARTUCCI, LUCIA; KARABATAS, LILIANA; JONES, NANA HAWA; HWA, VIVIAN; REVALE, SANTIAGO; VAZQUEZ, MARTIN; JASPER, HECTOR; KUMAR, ASHISH; DOMENE, HORACIO

De novo germline STAT3 mutations associated with severe IGF-I deficiency and multi-organ autoimmune disease in two unrelated patients

Sociedad Latinoamericana de Endocrinologia Pediatrica

Lugar: Puerto Varas; Año: 2015;

MARTUCCI, LUCIA; SCAGLIA, PAULA; KARABATAS, LILIANA; REY, RODOLFO; DOMENE, HORACIO; DOMENE, SABINA; JASPER, HECTOR

In vitro functional characterization of IGFALS gene variants found in ALS deficient or idiopathic short stature (ISS) children

European Society of Pediatric Endocrinology

Lugar: Barcelona; Año: 2015;

SCAGLIA, PAULA; KESELMAN, ANA; GUTIERREZ, MARIANA; DOMENE, SABINA; BLANCO, MIGUEL; SANGUINETTI, NORA; BEZRODNIK, LILIANA; DI GIOVANNI, DANIELA; CALDIROLA, MARIA SOLEDAD; MARTUCCI, LUCIA; KARABATAS, LILIANA; KUMAR, ASHISH; JONES, NANA HAWA; HWA, VIVIAN; REVALE, SANTIAGO; VAZQUEZ, MARTIN; JASPER, HECTOR; DOMENE, HORACIO

Severe IGFI deficiency and multiorgan autoimmune disease associated with novel germline STAT3 mutations

European Society of Pediatric Endocrinology

Lugar: Barcelona; Año: 2015;

SCAGLIA, PAULA; MARTUCCI, LUCIA; KARABATAS, LILIANA; KESELMAN, ANA; SPINOLA-CASTRO, ANGELA MARIA; BRASLAVSKY, DEBORA; BALLERINI, MARIA GABRIELA; ROPELATO, MARIA GABRIELA; MARTINEZ, ALICIA; BENGOLEA, SONIA; PITMAN, VIVIANA; DOMENE, SABINA; BERGADA, IGNACIO; REY, RODOLFO; DOMENE, HORACIO; JASPER, HECTOR

Gene-Dosage Effect of Igfals Gene Mutations on the IGF System

16th International Congress of Endocrinology & the Endocrine Society 96th Annual Meeting & Expo

Lugar: San Diego; Año: 2014;

MARTUCCI, LUCIA; SCAGLIA, PAULA; KARABATAS, LILIANA; REY, RODOLFO; DOMENE, HORACIO; DOMENE, SABINA; JASPER, HECTOR

In Vitro Impairment of Protein Synthesis and/or Secretion of IGFALS Gene Variants Characterized in ALS Deficient or Idiopathic Short Stature Children

SOCIEDAD LATINOAMERICANA DE. ENDOCRINOLOGÍA Pediatrica

Lugar: Playa del Carmen; Año: 2014;

SCAGLIA, PAULA; KESELMAN, ANA; MARTUCCI, LUCIA; KARABATAS, LILIANA; BALLERINI, MARIA GABRIELA; DOMENE, SABINA; RODRIGUEZ AZRAK, SOL; JASPER, HECTOR; DOMENE, HORACIO

Three ALS Deficient Patients in a Non Consanguineous Family Presenting Four Different IGFALS Gene Variants

SOCIEDAD LATINOAMERICANA DE. ENDOCRINOLOGÍA Pediatrica

Lugar: Playa del Carmen; Año: 2014;

SCAGLIA, PAULA; KESELMAN, ANA; MARTUCCI, LUCIA; KARABATAS, LILIANA; BALLERINI, MARIA GABRIELA; DOMENE, SABINA; ACOSTA, JOHANA; JASPER, HECTOR; DOMENE, HORACIO

ALS Deficiency due to a Novel and Two Already Described IGFALS Gene Mutations in an Unusual Non Consanguineous Family: Two Compound Heterozygous (Father and Son) and Two Heterozygous Carriers (Brother and Mother)

European Society for Pediatric Endocrinology

Lugar: Dublin; Año: 2014;

DOMENÉ SABINA

El pez cebra como modelo de Patologia Genetica Humana

XLIII CONGRESO ARGENTINO DE GENÉTICA IV REUNIÓN REGIONAL SAG-LA PAMPA PATAGONIA

Lugar: Bariloche; Año: 2014;

DANIELA ORQUERA; SOFIA NASIF; SABINA DOMENE; MALCOLM LOW; MARCELO RUBINSTEIN; FLAVIO JUNQUEIRA

Dissecting the function of the homeodomain transcription factor Rax during hypothalamic development

VI International Meeting of the Latin American Society for Developmental Biology

Lugar: Montevideo; Año: 2012;

SABINA DOMENE

El Pez Cebra como Modelo de Patología Humana.

XII Meeting of Brazilian Society of Laboratory Animal Science (SBCAL): Paradigms of Laboratory Animal Science and I Latin American Meeting: Amigos para Siempre

Lugar: Foz de Iguazu; Año: 2012;

DOMENE, SABINA; VIVIANA BUMASCHNY; FLAVIO JUNQUEIRA; MARCELO RUBINSTEIN

Proopiomelanocortin gene (Pomc) expression at the vertebrate extremes: cis/trans comparative studies in mouse and zebrafish

Latin American Zebrafish Network

Lugar: Rosario; Año: 2012;

SABINA DOMENE

El pez cebra como modelo de patologia humana

Reunion Anual Conjunta SAIC-SAFIS-AACYTAL

Lugar: Mar del Plata; Año: 2011;

FLAVIO JUNQUEIRA; DANIELA ORQUERA; SOFIA NASIF; SABINA DOMENE; MALCOLM LOW; MARCELO RUBINSTEIN

The homeodomain transcription factor Rx determines gene expression territories during early hypothalamic development

Gene Expression and RNA processing

Lugar: Cataratas del Iguazu; Año: 2011;

JORGE I VELEZ; SABINA DOMENE; ERICH ROESSLER; BENJAMIN FELDMAN; MAXIMILIAN MUENKE

Functional activity quantification of mutations in the human six3 Gene in holoprosencephaly

Sixth Annual NIH Graduate Student Research Symposium

Lugar: National Institutes of Health, Bethesda, Maryland, USA; Año: 2010;

SABINA DOMENE; FLAVIO JUNQUEIRA; VIVIANA BUMASCHNY; SOFIA NASIF; MARCELO RUBINSTEIN

Functional Comparative Genomics at the Vertebrate Extremes.

Sociedad Argentina de Investigacion Bioquimica y Biologia Molecular (SAIB)

Lugar: San Miguel de Tucuman, Argentina; Año: 2009;

SABINA DOMENE

The zebrafish as a model for human disease

III Reunion Cientifica Regional ICLAS, FESSACAL, ACCMAL-Biomodelos aplicados al desarrollo e innovacion tecnologica

Lugar: Montevideo, Uruguay; Año: 2009;

SABINA DOMENE

El pez cebra como modelo de enfermedades humanas

VI Jornada "Otras especies utilizadas en experimentacion cientifica"

Lugar: Sede de la Sociedad de Medicina Veterinaria; Año: 2009;

SABINA DOMENE; KENIA EL-JAICK; ERICH ROESSLER; FELICITAS LACBAWAN; BEN FELDMAN; MAXIMILIAN MUENKE

SIX3 mutations in Holoprosencephaly (HPE) are loss-of-function alleles.

XXXVII Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology (SBBq)

Lugar: Aguas de Lindoia, San Pablo, Brasil; Año: 2008;

SABINA DOMENE; KENIA EL-JAICK; ERICH ROESSLER; FELICITAS LACBAWAN; BEN FELDMAN; MAXIMILIAN MUENKE

SIX3 mutations in Holoprosencephaly (HPE) are loss-of-function alleles.

XLXII Reunión Anual de Sociedad Argentina de Investigaciones Clínicas 2007

Lugar: Mar del Plata, Argentina; Año: 2007;

SABINA DOMENE; KENIA EL-JAICK; ERICH ROESSLER; FELICITAS LACBAWAN; BEN FELDMAN; MAXIMILIAN MUENKE

SIX3 mutations in Holoprosencephaly (HPE) are loss-of-function alleles.

American Society of Human Genetics (ASHG) Meeting

Lugar: San Diego, California, USA; Año: 2007;

SABINA DOMENE; NAOKI NAKAYA; KENIA EL-JAICK; ERICH ROESSLER; FELICITAS LACBAWAN; STANISLAV TOMAREV; BEN FELDMAN; MAXIMILIAN MUENKE

Development of Two Functional Assays to Study SIX3 mutations in Holoprosencephaly (HPE).

Mid-Atlantic Regional Developmental Biology Meeting

Lugar: Princeton, New Jersey, USA; Año: 2007;

ARCOS-BURGOS MAURICIO; JAIN M; DOMENE S; SHIVELY S; WALLIS D; STANESCU H; KARKERA JD; ACOSTA MT; BERG K; KLETA R; ROESSLER E; VORTMEYER A; PINEDA D; PALACIO JD; LOPERA F; MEYER J; LESCH KP; BAILEY-WILSON JE; CASTELLANOS FX; MUENKE M

A common ancestral haplotype located at 4q13.2 confers susceptibility to ADHD.

National Human Genome Research Institute (NHGRI) Scientific Retreat

Lugar: Gettysburg, Pensylvannia, USA; Año: 2006;

SABINA DOMENE; MAIA OUSPENSKAIA; ERICH ROESSLER; ROBERT KRAUSS; MAXIMILIAN MUENKE

Mutational Screening of CDO using dHPLC in Holoprosencephaly (HPE) Patients.

National Human Genome Research Institute (NHGRI) Scientific Retreat

Lugar: Gettysburg, Pensylvannia, USA; Año: 2006;

SABINA DOMENE; MAIA OUSPENSKAIA; ERICH ROESSLER; ROBERT KRAUSS; MAXIMILIAN MUENKE

Mutational Screening of CDO using dHPLC in Holoprosencephaly (HPE) Patients.

American Society of Human Genetics (ASHG) Meeting

Lugar: New Orleans, Luisiana, USA; Año: 2006;

ARCOS-BURGOS MAURICIO; JAIN M; DOMENE S; SHIVELY S; WALLIS D; STANESCU H; KARKERA JD; ACOSTA MT; BERG K; KLETA R; ROESSLER E; VORTMEYER A; PINEDA D; PALACIO JD; LOPERA F; MEYER J; LESCH KP; BAILEY-WILSON JE; CASTELLANOS FX; MUENKE M

A common ancestral haplotype located at 4q13.2 confers susceptibility to ADHD.

American Society of Human Genetics (ASHG) Meeting

Lugar: New Orleans, Luisiana, USA; Año: 2006;

MOYA M. CHRISTIAN; GUTNISKY J. VIVIANA; RIVOLTA M. CARINA; DOMENÉ SABINA; VARELA VIVIANA; VONO-TONIOLO J; MEDEIROS-NETO GERALDO; TARGOVNIK M. HECTOR

Identification of two compound heterozygous mutations (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in a brazilian family with congenital goiter and defective thyroglobulin synthesis.

XVI Sociedad Latinoamericana de Enfermedades Tiroideas

Lugar: Villa Carlos Paz, Cordoba, Argentina; Año: 2003;

RIVOLTA M. CARINA; SEBASTIAN A. ESPERANTE; GRUNEIRO-PAPENDIECK LAURA; CHIESA ANA; MOYA M. CHRISTIAN; DOMENÉ SABINA; VARELA VIVIANA; TARGOVNIK M. HECTOR

Identification of five novel inactivating mutations in the human thyroid peroxidase gene responsible for congenital goiter and iodide organification defect.

XVI Sociedad Latinoamericana de Enfermedades Tiroideas

Lugar: Villa Carlos Paz, Cordoba, Argentina; Año: 2003;

GRUNEIRO-PAPENDIECK LAURA; CHIESA ANA; RIVOLTA M. CARINA; SEBASTIAN A. ESPERANTE; MOYA M. CHRISTIAN; DOMENÉ SABINA; VARELA VIVIANA; HEINRICH J J; TARGOVNIK M. HECTOR

Mutations of the thyroid peroxidase gene in patients with total iodide organification defect.

Sociedad Latinoamericana de Endocrinologia Pediatrica (SLEP); Sociedad Mexicana de Endocrinologia Pediatrica (SMEP)

Lugar: Cancun, Mexico; Año: 2003;

DOMENÉ SABINA; RIVOLTA M. CARINA; MOYA M. CHRISTIAN; VARELA VIVIANA; TARGOVNIK M. HECTOR

Genotipification of polymorphic markers in the human thyroglobulin gene. Evidence confirming the mutation R277X results from a founder effect.

XLVIII Reunión Anual de la Sociedad Argentina de Investigación Clínica (SAIC)

Lugar: Mar del Plata, Argentina; Año: 2003;

MOYA M. CHRISTIAN; GUTNISKY J. VIVIANA; DOMENÉ SABINA; CARON, PHILLIPPE; MEDEIROS-NETO, GERALDO; TARGOVNIK, HECTOR

Identification of three compound heterocygotes in the human thyroglobulin gene associated to goiter and congenital hypothyroidism.

XLVIII Reunión Anual de la Sociedad Argentina de Investigación Clínica (SAIC)

Lugar: Mar del Plata, Argentina; Año: 2002;

RIVOLTA M. CARINA; GRUNEIRO-PAPENDIECK LAURA; CHIESA ANA; DOMENÉ SABINA; VARELA VIVIANA; TARGOVNIK M. HECTOR

Identification of New Mutations in the Human Thyroid Peroxidase Gene.

IV Jornada Multidisciplinaria de la Sociedad Argentina de Biologia (SAB)

Lugar: IBIME, Buenos Aires, Argentina; Año: 2002;

RIVOLTA M. CARINA; GRUNEIRO-PAPENDIECK LAURA; CHIESA ANA; DOMENE, SABINA; TARGOVNIK M. HECTOR

Identification of new mutations in the human thyroperoxidase gene.

XLVIII Reunión Anual de la Sociedad Argentina de Investigación Clínica (SAIC)

Lugar: Mar del Plata, Argentina; Año: 2002;