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FRONTIERS IN GENETICS, ISSN 1664-8021, 07/2019, Volume 10, p. 425
Prenatal ultrasound (US) abnormalities often pose a clinical dilemma and necessitate facilitated investigations in the search of diagnosis. The strategy of... 
ultrasound abnormalities | whole-exome sequencing (WES) | ABNORMALITIES | clinical genetics | GENETICS & HEREDITY | congenital anomalies | FETUSES | prenatal diagnosis | Pregnant women | Family | Reports
Journal Article
Journal of Genetic Counseling, ISSN 1059-7700, 4/2016, Volume 25, Issue 2, pp. 314 - 324
Many factors predict the intention to disclose genetic information to relatives. The article examines the impact of patients’ socio-demographic factors on... 
Human Genetics | Ethics | Public Health | Biomedicine | Gynecology | Genetic information | Family | Clinical Psychology | Relatives | Israel | Disclosure | DIAGNOSIS | NONPOLYPOSIS COLORECTAL-CANCER | INFORMATION | HEREDITARY BREAST | RISK | RESPONSIBILITY | HEALTH COMMUNICATION | GENETICS & HEREDITY | MUTATIONS | PERCEPTIONS | Family - psychology | Genetic Counseling - psychology | Genetic Testing | Genetic Privacy - psychology | Humans | Middle Aged | Colorectal Neoplasms, Hereditary Nonpolyposis - psychology | Male | Socioeconomic Factors | Adult | Female | Surveys and Questionnaires | Neoplastic Syndromes, Hereditary - genetics | Neoplastic Syndromes, Hereditary - psychology | Genetic Predisposition to Disease - psychology | Genetic Predisposition to Disease - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Self Disclosure | Health Knowledge, Attitudes, Practice | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Breast Neoplasms - psychology | Aged | BRCA2 Protein - genetics | Diagnosis | Cancer | Sociodemographic aspects | Clinics | Demographic aspects | Susceptibility | Antenatal | Professional attitudes | Response rate | Social background | Families & family life | Attitudes | Counselling | Genetic screening | Screening | Genetic counseling | Motivation | Religious aspects | Socioeconomic factors | Genetic testing | Genetic factors
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 08/2019, Volume 39, Issue 9, pp. 751 - 757
Objective To determine the contribution of chromosomal microarray (CMA) and other advanced genetic tests to the genetic evaluation of fetal pleural effusion... 
HYDROTHORAX | RISK | NONIMMUNE HYDROPS-FETALIS | GENETICS & HEREDITY | OBSTETRICS & GYNECOLOGY | Evaluation | Effusion | Identification methods | Abnormalities | Fetuses | Karyotypes | Pleural effusion | Aneuploidy | Parameter identification | Multivariate analysis | Genetic screening | Gene sequencing | Genetic abnormalities | DNA microarrays | Anomalies
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 05/2019, Volume 39, Issue 6, pp. 477 - 483
Objective Data regarding the neurodevelopmental outcome of fetal short corpus callosum (CC) diagnosed according to standard reference charts is scarce. The... 
AGENESIS | GENETICS & HEREDITY | OBSTETRICS & GYNECOLOGY | Medicine, Experimental | Medical research | Pregnant women | Analysis | Pregnancy | Prenatal diagnosis | Statistical analysis | Fetuses | Charts | Children | Health risk assessment | Medical diagnosis | Reclassification | Corpus callosum
Journal Article
PRENATAL DIAGNOSIS, ISSN 0197-3851, 07/2016, Volume 36, Issue 7, pp. 650 - 655
ObjectiveThe purpose of our study was to describe the sonographic appearance of triploidy in early pregnancy. MethodsWe report the sonographic characteristics... 
FETAL TRIPLOIDY | CHROMOSOME-ABNORMALITIES | HELLP-SYNDROME | ULTRASOUND FINDINGS | FREE BETA-HCG | SPONTANEOUS-ABORTIONS | GENETICS & HEREDITY | PAPP-A | WEEKS GESTATION | PARENTAL ORIGIN | NUCHAL TRANSLUCENCY | OBSTETRICS & GYNECOLOGY | Pregnancy | Pregnant women | Chromosomes
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 07/2016, Volume 36, Issue 7, pp. 650 - 655
Journal Article
The Journal of Maternal-Fetal & Neonatal Medicine, ISSN 1476-7058, 05/2018, Volume 31, Issue 10, pp. 1285 - 1289
Purpose: One of the greatest challenges with the finding of adducted thumbs in the prenatal setting is the determination of whether this finding is associated... 
prenatal diagnosis | L1CAM | neurodevelopmental disorders | Adducted thumbs | ultrasound | HYDROCEPHALUS | OBSTETRICS & GYNECOLOGY
Journal Article
FRONTIERS IN GENETICS, ISSN 1664-8021, 12/2018, Volume 9, p. 606
Introduction: Fragile X syndrome (FXS) is a common form of X-linked intellectual and developmental disability with a prevalence of 1/4000-5000 in males and... 
risk assessment | FMR1 premutation | PRACTICE GUIDELINES | INSTABILITY | full mutation expansion | LENGTH | EXPANDED ALLELES | PREVALENCE | AGG interruptions | REGION | genetic counseling | REPEAT PRIMED PCR | carrier screening | GENE | CGG REPEAT | GENETICS & HEREDITY | FRAGILE-X-SYNDROME | Fragile X syndrome | Research | Gene mutations | Risk factors
Journal Article
Journal of Ultrasound in Medicine, ISSN 0278-4297, 07/2018, Volume 37, Issue 7, pp. 1827 - 1833
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 07/2016, Volume 36, Issue 7, pp. 650 - 655
Journal Article
European Journal of Radiology, ISSN 0720-048X, 04/2019, Volume 113, pp. 232 - 237
Arachnoid cysts (AC) are congenital lesions comprising 1% of all intracranial mass lesions. The aim of this study was to characterize arachnoid cysts and their... 
Arachnoid cyst | Supratentorial cyst | Fetal brain | Infratentorial cyst | Neurodevelopmental outcome | MRI | SUPRASELLAR | MANAGEMENT | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Diagnostic imaging | Genetic disorders | Cysts | Pregnant women
Journal Article