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Общее количество найденных документов : 46
Показаны документы с 1 по 20
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1.
| Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease // Prenat. Diagn., 1995. Vol. 15, N 6.-С.579-584
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2.
| Salvesen Douglas R. Early amniocentesis and fetal nuchal translucency in women requesting karyotyping for advanced maternal age // Prenat. Diagn., 1995. Vol. 15, N 10.-С.971-974
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3.
| Imagenes ecocardiograficas prenatales de un hidrops fetal no inmune con sindrome de Down y canal atrioventricular comun // Toko-ginecol. pract., 1995. Vol. 54, N 597.-С.83-85
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4.
| Cruger D.G. Quantitative evaluation of fluorescence in situ hybridization (FISH) signals in uncultured coelomic cells // Prenat. Diagn., 1997. Vol. 17, N 7.-С.635-642
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5.
| True fetal mosaicism of an isochromosome of the long arm of a chromosome 20: The dilemma persists // Prenat. Diagn., 1997. Vol. 17, N 12.-С.1171-1175
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| Strong preference for non-invasive prenatal diagnosis in women pregnant through intracytoplasmic sperm injection (ICSI) // Prenat. Diagn., 1998. Vol. 18, N 7.-С.700-705
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| Современные достижения молекулярный цитогенетики в диагностике хромосомной патологии у детей // Рос. вестн. перинатол. и педиатрии, 1998. Т. 43, N 1.-С.31-36
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| Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contrastructural arachnodactyly // Amer. J. Med. Genet., 1998. Vol. 77, N 3.-С.188-197
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| Pinson S. Syndrome polymalformatif, retard mental et remaniement telomerique (4;6) familial // Ann. genet., 1998. Vol. 41, N 4.-С.221
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| Sex chromosome pentasomy (49, XXXXY) presenting as cystic hygroma at 16 weeks' gestation // Prenat. Diagn., 1999. Vol. 19, N 3.-С.257-259
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| Sepulveda W. Two uncommon umbilical vessel anomalies in a fetus with trisomy 18 // Prenat. Diagn., 1998. Vol. 18, N 10.-С.1098-1099
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| Qumsiyeh Mazin B. Chromosome abnormalities in the placenta and spontaneous abortions // J. Maternal-Fetal Med., 1998. Vol. 7, N 4.-С.210-212
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| Stereotactically guided breast cor biopsy 910 cases // Abstr. 10th European Congress of Radiology - ECR'97, Vienna, Austria, March 2-7, 1997. -Amsterdam, 1997.-С.2-048
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14.
| Developmental analysis of cardiovascular system of 45, X fetuses with cystic hygroma // Amer. J. Med. Genet., 1997. Vol. 68, N 2.-С.135-141
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15.
| Severe fetal malformations associated with trisomy 16 confined to the placenta // Prenat. Diagn., 1997. Vol. 17, N 8.-С.777-779
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16.
| Stereotactically guided breast cor biopsy 910 cases // Abstr. 10th European Congress of Radiology - ECR'97, Vienna, Austria, March 2-7, 1997. -Amsterdam, 1997.-С.2-048
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17.
| Shioda K. A case of multiple mosaic aneuploidy in siblings // Teratology, 1998. Vol. 57, N 3.-С.22A
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18.
| Isolated sacral agenesis in a fetus monosomic for 7q36.1'->'qter // J. Med. Genet., 1997. Vol. 34, N 10.-С.866-868
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| Clinical course and outcome of fetal cystic hygroma diagnosed in the first or early second trimester // Teratology, 1998. Vol. 57, N 3.-С.12-13
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20.
| Kalousek Dagmar K. Pathogenesis of chromosomal mosaicism and its effect on early human development // Amer. J. Med. Genet., 2000. Vol. 91, N 1.-С.39-45
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