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;

RECALCATTI, MACARENA; SALATINO LUCIA; FERNANDEZ, MARIA CELIA; MARTIN, AYELEN; KESELMAN, ANA; DOMENE, HORACIO; PENNISI, PATRICIA; PLAZAS, PAOLA V; DOMENE, SABINA

Desarrollo de un ensayo funcional in vivo usando el modelo de pez cebra para evaluar la patogenicidad de dos variantes identificadas en el gen IGF1 en pacientes con talla baja

Zebrafish en Red

Lugar: Rosario; 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;