-
1
المؤلفون: I W, Lurie, I V, Novikova, O A, Tarletskaya, A A, Lazarevich, O A, Gromyko
المصدر: Genetic counseling (Geneva, Switzerland). 27(2)
مصطلحات موضوعية: Adult, Chromosomes, Human, Pair 13, Pregnancy, Humans, Abnormalities, Multiple, Abortion, Induced, Chromosome Disorders, Female, Neural Tube Defects, Chromosome Deletion, Ultrasonography, Prenatal
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::64b595340d34685881dc94a26f9122c3
https://pubmed.ncbi.nlm.nih.gov/29485808 -
2
المؤلفون: I W, Lurie
المصدر: Genetic counseling (Geneva, Switzerland). 26(4)
مصطلحات موضوعية: Humans, Abnormalities, Multiple, Female, Trisomy, Hirschsprung Disease
-
3
المؤلفون: I V, Novikova, A A, Lazarevich, T M, Egorova, I V, Solovyeva, E I, Golovataja, T A, Plevako, N G, Mikheeva, I W, Lurie
المصدر: Genetic counseling (Geneva, Switzerland). 25(1)
مصطلحات موضوعية: Adult, Fetal Growth Retardation, Limb Deformities, Congenital, Abortion, Induced, Gestational Age, Fetus, Pregnancy, Prenatal Diagnosis, Tetralogy of Fallot, Humans, Chromosomes, Human, Pair 6, Female, Genetic Testing, Chromosome Deletion, Ultrasonography
-
4
المؤلفون: I W Lurie, A I Vásquez-Velásquez, M G Domínguez, Horacio Rivera
المصدر: Cytogenetic and genome research. 141(1)
مصطلحات موضوعية: Adult, Male, Inheritance Patterns, Biology, Young Adult, Meiosis, Risk Factors, Chromosome instability, Chromosomal Instability, Chromosome Duplication, Prohibitins, Genetics, Chromosomes, Human, Humans, Molecular Biology, Small supernumerary marker chromosome, Genetics (clinical), X chromosome, Chromosomal inversion, Recombination, Genetic, Autosome, Age Factors, Telomere, Genetics, Population, Mutation (genetic algorithm), Chromosome Inversion, Mutation, Female, Ploidy, Chromosome Deletion
-
5
المؤلفون: N V, Nikitina, O A, Bushueva, E B, Nikolaeva, G V, Pavlov, I W, Lurie
المصدر: Genetic counseling (Geneva, Switzerland). 14(2)
مصطلحات موضوعية: Male, Chromosomes, Human, Pair 15, Child, Preschool, Karyotyping, Humans, Mothers, Genetic Predisposition to Disease, Ring Chromosomes, Syndrome
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::6170fc6d943ca7ae0a7d6cbc070c9aee
https://pubmed.ncbi.nlm.nih.gov/12872812 -
6
المؤلفون: I W, Lurie
المصدر: Genetic counseling (Geneva, Switzerland). 14(1)
مصطلحات موضوعية: Chromosome Aberrations, Gene Rearrangement, Hernia, Diaphragmatic, Chromosome Mapping, Humans, Abnormalities, Multiple, Trisomy, Syndrome, Chromosome Deletion, Aneuploidy
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::82101cc7c4f8c84583f5ffa4c78c09ff
https://pubmed.ncbi.nlm.nih.gov/12725592 -
7
المؤلفون: I W Lurie, V A Samochvalov
المصدر: British Journal of Ophthalmology. 78:415-417
مصطلحات موضوعية: medicine.medical_specialty, Eye disease, Aneuploidy, Trisomy, Cellular and Molecular Neuroscience, Ophthalmology, medicine, Humans, Microphthalmos, Uvea, Genetics, Coloboma, business.industry, Infant, Newborn, medicine.disease, Infant newborn, Sensory Systems, medicine.anatomical_structure, Female, Chromosomes, Human, Pair 4, business, Research Article
-
8Atrioventricular septal defects: possible etiologic differences between complete and partial defects
المؤلفون: C A, Loffredo, J, Hirata, P D, Wilson, C, Ferencz, I W, Lurie
المصدر: Teratology. 63(2)
مصطلحات موضوعية: Adult, Heart Septal Defects, Ventricular, Male, Infant, Newborn, Heart Septal Defects, Atrial, Diabetes, Gestational, Pregnancy, Risk Factors, Case-Control Studies, Baltimore, District of Columbia, Humans, Female, Down Syndrome
-
9
المؤلفون: D, Kotzot, I W, Lurie, K, Méhes, E, Werder, A, Schinzel
المصدر: Clinical genetics. 58(3)
مصطلحات موضوعية: Adult, Genetic Markers, Male, Parents, Fetal Growth Retardation, Haplotypes, Karyotyping, Chromosomes, Human, Humans, Female, Middle Aged, Aneuploidy, Child
-
10
المؤلفون: C A, Loffredo, C, Ferencz, P D, Wilson, I W, Lurie
المصدر: Teratology. 61(5)
مصطلحات موضوعية: Male, Likelihood Functions, Chromosomes, Human, Pair 22, Cleft Lip, Heart Septal Defects, Infant, Newborn, Infant, Aorta, Thoracic, Congenital Abnormalities, Cleft Palate, Risk Factors, Case-Control Studies, DiGeorge Syndrome, Humans, Abnormalities, Multiple, Female