No. | Poster Title |
---|---|
1 | ‘WHEN LIGHTNING STRIKES TWICE’ – PGT FOR TWO INDICATIONS IN ONE BIOPSY Einav Kremar; Tamar Krisher ; Assaf Ben-Meir; Efrat Esh-Broder; Mali Ketzinel Gilad Israel |
2 | 22Q11.2 MICRODUPLICATION: AN ENIGMATIC GENETIC DISORDER? CASE SERIES IN THE PRENATAL AND POSTNATAL SETTING AND REVIEW OF THE LITERATURE Agnese Feresin; Stefania Cappellani ; Carla Morando; Maria Teresa Bonati; Elisa Rubinato Italy |
3 | A CE-MARKED IVDD PREIMPLANTATION GENETIC ANALYSIS SOLUTION OF ANEUPLOIDIES IN EMBRYOS Alain Rico; Adam Harris; Berthe Youness France |
4 | CARRIER GENETIC SCREENING OF AUTOSOMAL RECESSIVE AND X-LINKED DISEASES IN ARAB POPULATION Ana Bover; Julio C. Martín; María Lairon; Joaquín Panadero; Ana Cervero; Carlos Simón Spain |
5 | COMPARISON OF PGT-SR RESULTS IN CARRIERS OF DIFFERENT BALANCED CHROMOSOMAL REARRANGEMENTS. Yulia Rumyantseva; Ekaterina Vasileva; Natalia Isaeva; Roman Bikanov Russian Federation |
6 | COMPUTER ASSISTED GENETIC COUNSELING FOR EXPANDED CARRIER SCREENING Adi Reches; Yuval Yaron; Vered Ofen Glassner; Michal Berkenstadt; Nurit Goldstein; Haike Reznik Israel |
7 | CONVEYING RECURRENCE RISK FOR AN APPARENT DE NOVO PATHOGENIC VARIANT: WHAT SHOULD BE THE COUNSELING? Annick Rein-Rothschild; Ben Pode-Shakked; Odelia Chorin Israel |
8 | CRYPTIC MATERNAL MOSAICISM ASSOCIATED WITH RECURRENT ATYPICAL PRENATAL CELL-FREE DNA SCREENING RESULTS IN CONSECUTIVE PREGNANCIES Kristen Miller; Karin J. Blakemore; Jaclyn B. Murry USA |
9 | DEVELOPING A BIOINFORMATICAL “PROOFREADING” METHOD FOR CNV RESULTS IN NIPGT Gábor L. Kovács; Gombos Katalin ; Bence Gálik; Hungary |
10 | DNA CONCENTRATIONS IN AMNIOTIC FLUID ACCORDING TO GESTATIONAL AGE AND FETAL SEX – DATA FROM 2,573 SAMPLES Yoel Gofin; RAN Svirsky ; Dana Lavi Ben Atav; Meytal Liberman; Tamar Tenne Israel |
11 | EARLY MID-TRIMESTER GENETIC SONOGRAPHY FOR DETECTING FETAL STRUCTURAL ANOMALIES: THE BEST OF ALL WORLDS Rachel Michaelson; Yehudit Zangi; Ari Weiss; Hen Sela; Israel |
12 | EXPANDING THE PHENOTYPE OF CONGENITAL HEART DEFECTS RELATED TO GATA TRANSCRIPTION FACTORS FAMILY – CASE REPORT OF TWO PRENATAL CASES Joaquim Sá; Mafalda Simões ; Miguel Branco; Filipa Nunes; Eulália Galhano Portugal |
13 | IDENTIFICATION OF BALANCED TRANSLOCATION EMBRYOS DERIVED FROM COUPLES WITH RECIPROCAL AND ROBERTSONIAN TRANSLOCATIONS BY KARYOMAPPING Sirikul Kulanuwat; Wanwisa Suksalak; Patthorn Jaikla; Nadsarin Tochoowong; Wipawee Tangsri; ChutimonPomsuwan Thailand |
14 | IMMUNOLOGICAL CHARACTERIZATION AND MOLECULAR DETERMINATION OF PRO-INFLAMMATORY CYTOKINE BIOMARKERS IN PCOS WOMEN OF SAUDI ARABIA Arwa Alageel Saudi Arabia |
15 | MAPPING THE PREVALENCE AND ORIGIN OF (MOSAIC) CHROMOSOMAL ABNORMALITIES IN HUMAN BLASTOCYSTS: FINDINGS AND POTENTIAL VALUE FOR PGT Machteld Baetens; Lisa De Witte; Kelly Tilleman; FraukeVanden Meerschaut; Sandra Janssens; Ariane Van Tongerloo; Belgium |
16 | PREIMPLANTATION GENETIC TESTING FOR ANEUPLOIDIES AND STRUCTURAL REARRANGEMENTS OF POLAR BODIES USING THE EMBRYOMAP PLATFORM Lena Walenta; Maryna Pohorila; Ana Bellón; Katarzyna Osetek-Müller; Annett Wagner; Lisa Peterson Germany |
17 | SHORT TANDEM REPEAT MARKERS PROPERLY IDENTIFIED EUPLOID EMBRYO DEVELOPED FROM TRIPRONUCLEAR (3PN) ZYGOTE Sirikul Kulanuwat; Wanwisa Suksalak; Wipawee Tangsri; Patthorn Jaikla; Nadsarin Tochoowong; ChutimonPomsuwan Thailand |
18 | SHOULD ABNORMAL FETUSES BE PRESERVED? – A VIEW FROM GENE EXPRESSION IN FETAL AND ADULT STEM CELLS Elizabeth Lau; Mary Tang Australia |
19 | SNP-ARRAY ANALYSIS IN RECURRENT PREGNANCY LOSS: INSIGHTS FROM A RETROSPECTIVE STUDY Sheila Ulivi; Adamo Pio D’Adamo; Elisa Paccagnella; Beatrice Spedicati; Stefania Zampieri; Diego Favretto ; Giovanni Turchetto; Davide De Santo; Gianpaolo Maso; Giorgia Girotto; Paolo Gasparini; Stefania Cappellani Italy |
20 | THE CLINICAL APPLICATION OF GENOME-WIDE KARYOMAPPING FOR MONOGENIC DISEASES AND ANEUPLOIDY IN PREIMPLANTATION IVF EMBRYOS Tanarut K .Jantapanon; Kasorn Tiewsiri; Piyarat Thaijaroen; Sarinee Pingsuthiwong; Thannop Supaksathapronpun; Ruthairat Kerdkaew Thailand |
21 | THE DETECTABILITY OF PAIRED-END SEQUENCING-BASED NONINVASIVE PRENATAL TESTING IN SAMPLES WITH LOW FETAL FRACTION: REPORT OF THREE CASES Kulvadee Tangmansakulchai; Sasithorn Promwan; Chollada Wetchwikool; Sujin Chanchamroen; Wiwat Quangkananurug; Thailand |
22 | PRENATAL DIAGNOSIS BALANCED TRANSLOCATION AND AN UNEXPECTED FINDING IN CHROMOSOMAL MICROARRAY ANALYSIS Osvaldo Moutinho; Márcia Martins ; Rosário Pinto Leite Portugal |
Poster ListAdam Barkay2024-05-16T06:39:10+00:00