All screenings for gene PALB2

98 entries on 1 page. Showing entries 1 - 98.
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Variants found     

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0000000109 00000100 DNA SEQ-NG Dasa Genómica - Genia;INVITAE Invitae Breast Cancer Panel 20-apr-2017 Multigenetic panel 20 Lina Nuñez-Private Practice
0000000197 00000173 DNA SEQ-NG Sanatorio Allende Breast Cancer Panel 2-may-2017 - 2 Norma Rossi-Hospital de Córdoba
0000000205 00000180 DNA SEQ CEMIC Known familial mutation 24-may-2017 - 1 Alejandra Mampel-Hospital Universitario de Mendoza
0000000209 00000184 DNA SEQ-NG;z-score-CNV Héritas Panel Héritas (12 genes) 23-may-2017 - 21 Alejandra Mampel-Hospital Universitario de Mendoza
0000000229 00000202 DNA SEQ-NG;z-score-CNV Héritas Panel Héritas (12 genes) 13-oct-2016 - 6 Laura Vargas Roig-IMBECU
0000000259 00000225 DNA SEQ-NG;z-score-CNV Héritas Panel Héritas (9 genes) 12-jan-2017 - 18 Lina Nuñez-Hospital Alemán
0000000284 00000243 DNA SEQ-NG Dasa Genómica - Genia;INVITAE Invitae Breast Cancer Panel 31-jul-2017 Multigenetic panel 1 Norma Rossi-Hospital de Córdoba
0000000424 00000371 DNA SEQ-NG IACA CNVs screening for BRCA1, BRCA2, PALB2 14-sep-2017 - 18 Alejandra Mampel-Hospital Universitario de Mendoza
0000000432 00000379 DNA SEQ-NG;z-score-CNV Héritas Panel Héritas (8 genes) 10-mar-2017 Multigenetic panel 10 Gonzalo Tabares-CEMA
0000000433 00000380 DNA SEQ-NG STEM Panel Cáncer de mama-ovario Hereditario STEM (11 genes) 1-nov-2017 - 1 Gonzalo Tabares-CEMA
0000000449 00000396 DNA SEQ-NG;z-score-CNV Héritas - 21-jul-2017 Multigenetic panel 28 Gonzalo Tabares-CEMA
0000000459 00000406 DNA SEQ-NG;z-score-CNV Héritas - 19-jul-2017 Multigenetic panel 25 Gonzalo Tabares-CEMA
0000000460 00000407 DNA SEQ-NG;z-score-CNV Héritas - 22-oct-2017 Multigenetic panel 8 Gonzalo Tabares-CEMA
0000000461 00000408 DNA SEQ-NG STEM - 29-nov-2017 Multigenetic panel 1 Gonzalo Tabares-CEMA
0000000462 00000409 DNA SEQ-NG;z-score-CNV Héritas - 25-jul-2017 Multigenetic panel 16 Gonzalo Tabares-CEMA
0000000463 00000410 DNA SEQ-NG;z-score-CNV Héritas Panel Héritas (10 genes) 10-ago-2017 - 5 Gonzalo Tabares-CEMA
0000000464 00000411 DNA SEQ-NG;z-score-CNV Héritas - 22-aug-2017 Multigenetic panel - Gonzalo Tabares-CEMA
0000000468 00000414 DNA SEQ-NG STEM Panel STEM (11 genes) 18-dic-2017 Multigenetic panel 1 Gonzalo Tabares-CEMA
0000000503 00000446 DNA SEQ-NG Héritas Panel Héritas (12 genes) 21-sep-2017 - 4 Laura Vargas Roig-IMBECU
0000000506 00000449 DNA SEQ-NG Héritas Panel Héritas (12 genes) 19-jul-2017 - 13 Laura Vargas Roig-IMBECU
0000000510 00000453 DNA SEQ-NG Héritas Panel Héritas (12 genes) 14-aug-2017 - 5 Laura Vargas Roig-IMBECU
0000000561 00000497 DNA SEQ-NG CEMIC Panel CEMIC 3-jan-2018 - 18 Pablo Kalfayan-Hospital Italiano
0000000681 00000594 DNA SEQ-NG IACA CNVs screening for BRCA1, BRCA2, PALB2, RAD51D, RAD51C, TP53 4-may-2018 Multigenetic panel 1 Lina Nuñez-Private Practice
0000000753 00000651 DNA SEQ-NG;z-score-CNV Héritas - 30-jul-2018 Multigenetic panel 1 Alvaro Yanzi-Instituto San Marcos
0000000817 00000506 DNA SEQ-NG CEMIC - 21-may-2018 Multigenetic panel 13 Lina Nuñez-Private Practice
0000000991 00000838 DNA SEQ-NG CEMIC - 21-mar-2019 Multigenetic panel 18 Lina Nuñez-Private Practice
0000001048 00000883 DNA SEQ Hospital Privado Centro Médico de Córdoba - 21-nov-2018 Known familial mutation 2 Cecilia Montes-IMGO
0000001133 00000939 DNA CNVs;SEQ-NG IACA - 14-mar-2019 Multigenetic panel 13 Silvina Sisterna-Hospital de Comunidad
0000001135 00000941 DNA SEQ-NG CEMIC - 21-mar-2019 Multigenetic panel 11 Dolores Mansilla-Instituto Roffo
0000001141 00000946 DNA SEQ-NG CEMIC - 24-apr-2019 Multigenetic panel 2 Dolores Mansilla-Instituto Roffo
0000001157 00000960 DNA CNVs;SEQ-NG Héritas - 26-jul-2019 Multigenetic panel 1 Claudia Martin-Hospital de Córdoba
0000001229 00001024 DNA CNV;SEQ-NG IACA CNV in genes BRCA1, BRCA2, PALB2, RAD51D, RAD51C, TP53 26-sep-2018 Multigenetic panel 27 Silvina Sisterna-Hospital de Comunidad
0000001254 00001048 DNA SEQ-NG CEMIC - 4-aug-2019 Multigenetic panel 15 Claudia Martin-Hospital de Córdoba
0000001283 00001072 DNA CNV;SEQ-NG IACA - 4-oct-2019 Multigenetic panel 24 Silvina Sisterna-Hospital de Comunidad
0000001284 00001073 DNA CNV;SEQ-NG IACA - 27-dec-2019 Multigenetic panel 20 Silvina Sisterna-Hospital de Comunidad
0000001393 00001166 DNA CNV;SEQ-NG Invitae (deriv. Genia) - 24-oct-2019 Multigenetic panel 1 Pablo Kalfayan-Hospital Italiano
0000001407 00001177 DNA CNV;SEQ-NG Hospital Universitario Austral Test realizado en Laboratorio de Derivación 28-jan-2020 Multigenetic panel 1 Pablo Kalfayan-Hospital Italiano
0000001497 00001258 DNA CNV;SEQ-NG IACA - 9-dec-2019 Multigenetic panel 15 Silvina Sisterna-Hospital de Comunidad
0000001514 00001275 DNA CNV;SEQ-NG IACA - 15-apr-2019 Multigenetic panel 18 Silvina Sisterna-Hospital de Comunidad
0000001516 00001277 DNA CNV;SEQ-NG IACA - 29-jul-2019 Multigenetic panel 31 Silvina Sisterna-Hospital de Comunidad
0000001517 00001278 DNA SEQ-NG IACA CNV analysis of BRCA1, BRCA2, PALB2, RAD51D, RAD51C and TP53 26-sep-2018 Multigenetic panel 24 Silvina Sisterna-Hospital de Comunidad
0000001524 00001285 DNA CNV;SEQ-NG IACA CNV test of BRCA1, BRCA2, PALB2, RAD51C, RAD51D, TP53. 2-aug-2018 Multigenetic panel 32 Silvina Sisterna-Hospital de Comunidad
0000001530 00001291 DNA CNV;SEQ-NG IACA - 18-jun-2019 Multigenetic panel 20 Silvina Sisterna-Hospital de Comunidad
0000001533 00001294 DNA CNV;SEQ-NG IACA CNV test of BRCA1, BRCA2, PALB2, RAD51D, RAD51C, TP53 26-sep-2018 Multigenetic panel 23 Silvina Sisterna-Hospital de Comunidad
0000001534 00001295 DNA CNV;SEQ-NG IACA - 24-sep-2019 Multigenetic panel 25 Silvina Sisterna-Hospital de Comunidad
0000001540 00001301 DNA CNV;SEQ-NG IACA - 18-jun-219 Multigenetic panel 12 Silvina Sisterna-Hospital de Comunidad
0000001542 00001303 DNA CNV;SEQ-NG IACA - 21-oct-2019 Multigenetic panel 21 Silvina Sisterna-Hospital de Comunidad
0000001543 00001304 DNA CNV;SEQ-NG IACA - 7-may-2019 Multigenetic panel 22 Silvina Sisterna-Hospital de Comunidad
0000001584 00001343 DNA CNV;SEQ-NG Invitae (deriv. Genesia) - 19-dec-2019 Multigenetic panel - Dolores Mansilla-Instituto Roffo
0000001596 00001351 DNA SEQ-NG CEMIC - 9-sep-2019 Multigenetic panel 20 Dolores Mansilla-Instituto Roffo
0000001616 00001367 DNA SEQ Hospital Privado Centro Médico de Córdoba - 17-apr-2020 Known familial mutation - Claudia Martin-Hospital de Córdoba
0000001626 00001377 DNA SEQ Hospital Privado Centro Médico de Córdoba - 17-apr-2020 Known familial mutation 1 Claudia Martin-Hospital de Córdoba
0000001627 00001378 DNA SEQ Hospital Privado Centro Médico de Córdoba - 17-apr-2020 Known familial mutation 1 Claudia Martin-Hospital de Córdoba
0000001688 00001434 DNA CNV;SEQ-NG Héritas - 28-sep-2019 Multigenetic panel 2 Erika Stegmayer-CIOC
0000001693 00001439 DNA CNV;SEQ-NG Héritas - 5-jul-2017 Multigenetic panel 16 Laura Vargas Roig-IMBECU
0000001741 00001475 DNA SEQ-NG Domeq&Lafage - 4-may-2020 Multigenetic panel 12 Lina Nuñez-Hospital Alemán
0000001759 00001490 DNA SEQ-NG CEMIC - 25-sep-2019 Multigenetic panel 20 Erika Stegmayer-Inst. Nuestra Señora de las Mercedes
0000001760 00001491 DNA SEQ-NG Domeq&Lafage - 10-oct-2019 Multigenetic panel 19 Erika Stegmayer-CIOC
0000001761 00001492 DNA CNV;SEQ-NG Héritas - 31-oct-2019 Multigenetic panel 2 Erika Stegmayer-CIOC
0000001805 00001533 DNA SEQ-NG CEMIC - 3-oct-2019 Multigenetic panel 29 Dolores Mansilla-Instituto Roffo
0000001816 00001543 DNA SEQ-NG Biogenotec - 14-oct-2020 Multigenetic panel 1 Alejandra Mampel-COIR
0000001835 00001562 DNA SEQ-NG Biogenotec - 13-may-2021 Multigenetic panel 1 Alejandra Mampel-COIR
0000001836 00001563 DNA SEQ-NG Biogenotec - 03-feb-2020 Multigenetic panel 1 Alejandra Mampel-Hospital Universitario de Mendoza
0000001944 00001669 DNA SEQ-NG IACA Panel (13 genes) ATM, BARD1, BRCA1, BRCA2, BRIP1, CHEK2, NBN, PALB2, PTEN,RAD51C, RAD51D, STK11,TP53 27-jan-2021 Multigenetic panel 2 Silvina Sisterna-Hospital de Comunidad
0000001953 00001678 DNA SEQ Biogenotec Sanger Mutación puntual PALB2 y TP53 23-mar-2020 Specific pathology 1 Alejandra Mampel-COIR
0000001954 00001679 DNA SEQ-NG Biogenotec Panel Cáncer de mama y ovario DE 14 GENES (ATM, BRCA1, BRCA2, BRIP1, CHEK2, MLH1, MSH2, MSH6, NBN,PALB2, PMS2, PTEN, STK11, TP53) 29-oct-2020 Multigenetic panel 2 Alejandra Mampel-COIR
0000002011 00001732 DNA SEQ-NG CIBIC/Héritas Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53 23-jan-2018 Multigenetic panel 1 Instituto Nacional del Cancer
0000002013 00001734 DNA SEQ-NG CIBIC/Héritas Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53 04-oct-2018 Multigenetic panel 1 Marcela Lopez-CEMAFE
0000002021 00001742 DNA SEQ-NG CIBIC/Héritas Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53 20-jul-2018 Multigenetic panel 1 Marcela Lopez-CEMAFE
0000002028 00001749 DNA SEQ-NG IACA Panel (13 genes) ATM, BARD1, BRCA1, BRCA2, BRIP1, CHEK2, NBN, PALB2, PTEN,RAD51C, RAD51D, STK11,TP53 01-jan-2020 Multigenetic panel 2 Luisina Bruno-Instituto Fleming
0000002063 00001783 DNA SEQ-NG CEMIC Panel (11 genes) ATM, BRCA1, BRCA2, BARD1, CHEK2, MSH6, NBN, PALB2,PTEN, RAD51C, RAD51D. 22-jul-2021 Multigenetic panel 1 Jose Llugdar-IMOC
0000002087 00001802 DNA SEQ-NG Hospital Universitario Austral Panel (15 genes) ATM, BRCA1, BRCA2, CHEK2, CDH1, EPCAM, MLH1, MSH2, MSH6, NBN, PALB2, PMS2, PTEN, STK11, TP53 02-mar-2021 Multigenetic panel 1 Maria Constanza Vallone-Hospital Austral
0000002117 00001832 DNA SEQ-NG Genia/Invitae Panel cancer mama (12 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, STK11, TP53 01-sep-2021 Multigenetic panel 1 Pablo Kalfayan-Hospital Italiano
0000002161 00001875 DNA SEQ-NG IACA - 15-sep-2021 Multigenetic panel - Silvina Sisterna-Hospital de Comunidad
0000002278 00001991 DNA SEQ Fundación para el Progreso de la Medicina Analisis de variante: PALB2(NM_024675.4) c.2964del (p.Val989Ter) 22-jul-2021 Known familial mutation 1 Cecilia Montes-IMGO
0000002353 00002066 DNA SEQ-NG Invitae Invitae Breast Cancer Panel (13 genes) ATM*, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NF1*, PALB2, PTEN*, RAD51C, RAD51D, STK11, TP53 26-may-2022 Multigenetic panel Not yet submitted Lina Nuñez-Private Practice
0000002388 00002101 DNA SEQ-NG Fares Taie Panel Cancer mama-ovario (12 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53. 19-aug-2022 Multigenetic panel - Silvina Sisterna-Hospital de Comunidad
0000002390 00002103 DNA SEQ-NG Fares Taie Panel Cancer mama-ovario (12 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53. 24-aug-22 Multigenetic panel 2 Silvina Sisterna-Hospital de Comunidad
0000002405 00002118 DNA SEQ-NG Fares Taie Panel Cancer mama-ovario (10 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51D, TP53. 05-sep-2022 Multigenetic panel - Silvina Sisterna-Hospital de Comunidad
0000002412 00002125 DNA SEQ-NG Fares Taie Sindrome cáncer hereditario mama y ovarios (13 genes) ATM, BRCA1, BRCA2, BRIP1, EPCAM, MLH1, MSH2, MSH6, PALB2, PMS2, RAD51C, RAD51D, STK11 28-jul-2021 Multigenetic panel 1 Lina Nuñez-Private Practice
0000002457 00002166 DNA SEQ-NG Genesia - Progenitest;Instituto Alexander Fleming;INVITAE - 01-06-2022 Multigenetic panel - Lina Nuñez-Private Practice
0000002461 00002170 DNA SEQ-NG Fares Taie HP-SI-229-CIA 10-11-2022 Multigenetic panel - Silvina Sisterna-Hospital de Comunidad
0000002467 00002176 DNA SEQ IACA - 23-09-22 Known familial mutation 1 Silvina Sisterna-Hospital de Comunidad
0000002468 00002177 DNA SEQ-NG MEDgenomica - 22-09-22 Specific pathology 1 Silvina Sisterna-Hospital de Comunidad
0000002498 00002206 DNA SEQ-NG Fares Taie - 12-12-22 Specific pathology - Silvina Sisterna-Hospital de Comunidad
0000002512 00002219 DNA SEQ-NG Fares Taie Panel (11 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, TP53 22-12-22 Multigenetic panel 1 Silvina Sisterna-Hospital de Comunidad
0000002516 00002223 DNA SEQ-NG Fares Taie Panel (11 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, TP53 29-12-22 Multigenetic panel - Silvina Sisterna-Hospital de Comunidad
0000002519 00002226 DNA SEQ-NG Hospital Privado Centro Médico de Córdoba PROSTATE CANCER PANEL (12 genes) ATM, BRCA1, BRCA2, CHEK2, EPCAM, MLH1, MSH2, MSH6, NBN, PALB2, PMS2, RAD51D, TP53 28-10-22 Multigenetic panel - Claudia Martin-Hospital de Córdoba
0000002549 00000506 DNA SEQ-NG CEMIC complete gene sequencing: BRCA1, BRCA2, TP53, PTEN, STK11, CHEK2, PALB2, ATM, NBN 20-09-18 Multigenetic panel 1 Lina Nuñez-Private Practice
0000002550 00002256 DNA SEQ-NG CEMIC complete gene sequencing: BRCA1, BRCA2, TP53, PTEN, STK11, CHEK2, PALB2, ATM, NBN 04-10-19 Multigenetic panel - Lina Nuñez-Private Practice
0000002642 00002382 DNA SEQ-NG Laboratorio Fares Taie Breast and ovarian, BRCA1, BRCA2, PALB2 13-04-23 Specific pathology - Silvina Sisterna-Hospital de Comunidad
0000002678 00002303 DNA SEQ CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS NM_024675.4:c.1653T>A (p.Tyr551Ter) , gen PALB2 12-10-22 Known familial mutation 1 Emilia Maldonado-Hospital de Córdoba
0000002693 00002407 DNA SEQ-NG;arrayCNV Biocodices S.A. - 15-06-22 Multigenetic panel 2 Erika Stegmayer-CIOC
0000002697 00002411 DNA SEQ-NG CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS Panel (10 genes) ATM, BRCA1, BRCA2, CDH1, CHEK2, NBN, PALB2, PTEN, STK11, TP53 23-09-21 Multigenetic panel 1 Erika Stegmayer-CIOC
0000002791 00002489 DNA SEQ-NG CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS Hereditary Cancer panel (14 genes) ATM, BRCA1, BRCA2, CHEK2, EPCAM, HOXB13, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, RAD51C, RAD51D. 2-jun-2022 Multigenetic panel - Yolanda Isabel Medina - Hospital Juan D. Perón
0000002821 00002520 DNA SEQ Fundación para el Progreso de la Medicina secuenciacion sanger. PALB2 (NM_023675.3): c.1653T>A 16-mar-2023 Known familial mutation - Norma Rossi - Sanatorio Allende
0000002897 00002598 DNA SEQ-NG Fundación para el Progreso de la Medicina PALB2, exon 5 c.1965dup (p.(Pro656Serfs*7)) 20-04-23 Known familial mutation 1 Norma Rossi - Fundacion Para el Progreso de la Medicina
0000002918 00002618 DNA SEQ-NG Fundación para el Progreso de la Medicina - 27-mar-2023, 29-8-2023 Specific pathology Not yet submitted Norma Rossi - Sanatorio Allende
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