Keyphrases
Medical Center
100%
Israel
92%
Down Syndrome
69%
Lymphocytes
64%
Termination of Pregnancy
63%
Prenatal Diagnosis
59%
Fetal Abnormalities
56%
Turner Syndrome
51%
Aneuploidy
47%
X Chromosome
45%
Neonate
43%
Israeli
42%
Founder mutation
39%
Duplication
38%
Fluorescence in Situ Hybridization
36%
Jewish
36%
Ashkenazi Jews
35%
Clinical Presentation
35%
Assaf
34%
Intellectual Disability
32%
Replication Timing
31%
Singleton Pregnancy
31%
BRCA1, BRCA2
30%
Codon
30%
Trisomy 21
30%
Fetus
30%
Second Trimester
29%
Genotype
27%
Malformation
27%
Aristaless-related Homeobox
27%
Asynchronous Replication
27%
Nondisjunction
27%
Primary Ciliary Dyskinesia
27%
Ornithine Transcarbamylase Deficiency
27%
Deafness
27%
Neurodevelopmental Disorders
27%
Iraqi Jews
23%
Early Termination
23%
Breast Cancer Susceptibility Gene 1 (BRCA1)
23%
Developmental Delay
23%
Nuchal Translucency
23%
Asynchronously
22%
Mosaicism
22%
Clinical Spectrum
22%
Genotype-phenotype Correlation
22%
Screening Test
21%
Autosomal Recessive
20%
Proband
20%
Asynchrony
20%
Multiple Malformations
20%
Biochemistry, Genetics and Molecular Biology
Mosaicism
77%
Genetics
67%
Lymphocyte
65%
Allele
64%
Genotyping
59%
Aneuploidy
56%
Turner Syndrome
55%
Down Syndrome
53%
X Chromosome
49%
Exon
45%
Proband
42%
BRCA1
40%
Fluorescence in Situ Hybridization
40%
Trisomy
35%
Progeny
34%
Replication Timing
31%
Autosomal Dominant Inheritance
30%
Polymerase Chain Reaction
29%
Second Trimester Pregnancy
28%
Monosomy
27%
Phytohaemagglutinin
27%
Trisomy 21
27%
Primary Ciliary Dyskinesia
27%
Ornithine Transcarbamylase
27%
Nondisjunction
27%
Body Height
27%
Aristaless Related Homeobox
27%
Homeobox Gene
27%
Autosomal Recessive Inheritance
25%
DNA Sequence
23%
Codon
22%
Homozygosity
21%
Messenger RNA
21%
Pseudoautosomal Region
20%
Chromosome 21
20%
Fibroblast
20%
Genotype Phenotype Correlation
20%
Intellectual Disability
19%
Pregnancy
19%
First Trimester Pregnancy
19%
Cytogenetics
19%
Screening Test
18%
Chromosome Abnormality
18%
Splice Site Mutation
18%
Gene Frequency
18%
Human Chorionic Gonadotropin
17%
Haploinsufficiency
17%
Nonsense-Mediated Decay
17%
Awareness
17%
Gene Mutation
17%
Medicine and Dentistry
Fetal Disease
56%
Pregnancy
55%
Disease
54%
Prenatal Diagnosis
49%
Neonate
40%
Down Syndrome
33%
Infection
31%
Chromosome Aberration
28%
Congenital Malformation
28%
Brain Malformation
27%
Mosaicism
24%
Gestational Age
23%
Genetic Disorder
22%
Polymerase Chain Reaction
22%
Cleft Palate
22%
Skeleton Malformation
20%
Trisomy 21
20%
Child
20%
Exon
20%
BRCA1
20%
Gastrointestinal Bleeding
20%
Maternal Age
19%
Childbirth
18%
Second Trimester Pregnancy
17%
Neonatal Intensive Care Unit
17%
Maternal Serum
17%
Neonatal Infant
15%
Ovarian Cancer
15%
First Trimester Pregnancy
15%
Genetic Counseling
15%
Intracytoplasmic Sperm Injection
15%
Developmental Delay
14%
Fluorescence in Situ Hybridization
13%
Oocyte
13%
Third Trimester Pregnancy
13%
Frameshift Mutation
13%
Cone Rod Dystrophy
13%
Cytomegalovirus
13%
Preimplantation Genetic Diagnosis
13%
Sex Determination
13%
SCN3A
13%
Trisomy
13%
Ovarian Hyperstimulation Syndrome
13%
Chromosome 21
13%
Ascites
13%
Hypoplasia
13%
Splenomegaly
13%
Ranitidine
13%
Triploidy
13%
High Myopia
13%
