Поисковый запрос: (<.>S=КАРИОТИП ПЛОДА<.>) |
Общее количество найденных документов : 46
Показаны документы с 1 по 20
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1.
| A case of discordant related abnormal karyotypes form chorionic villi and amniocytes // Prenat. Diagn., 1999. Vol. 19, N 9.-С.887-890
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2.
| Shioda K. A case of multiple mosaic aneuploidy in siblings // Teratology, 1998. Vol. 57, N 3.-С.22A
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| Reddy K.S. A paternally inherited terminal deletion, del(8)(p23.1)pat, detected prenatally in an amniotic fluid sample: A review of deletion 8p23.1 cases // Prenat. Diagn., 1999. Vol. 19, N 9.-С.868-872
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| An unusual case of trisomy and triploidy in a chorion villus biopsy // Prenat. Diagn., 2000. Vol. 20, N 11.-С.917-920
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| An unusual case of trisomy and triploidy in a chorion villus biopsy // Prenat. Diagn., 2000. Vol. 20, N 11.-С.917-920
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| Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2) // Prenat. Diagn., 1999. Vol. 19, N 8.-С.783-786
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7.
| 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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| Chromosome analysis of human day 5 embryos // Genet. Res., 2000. Vol. 76, N 2.-С.204
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9.
| 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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| Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies // Prenat. Diagn., 2001. Vol. 21, N 8.-С.613-618
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11.
| 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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12.
| 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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13.
| First-trimester non-invasive prenatal diagnosis of triploidy // Prenat. Diagn., 1999. Vol. 19, N 2.-С.175-177
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14.
| 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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15.
| 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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16.
| Maternal uniparental isodisomy for chromosome 14 detected prenatally // Prenat. Diagn., 1999. Vol. 19, N 7.-С.681-684
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17.
| 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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18.
| Pilot models of preimplantation genetic diagnosis by PCR and FISH in human gametes and cleaving embryos // Докл. Бълг. АН, 1999. Vol. 52, N 9-10.-С.107-110
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19.
| Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7) // Prenat. Diagn., 2001. Vol. 21, N 8.-С.642-648
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20.
| Pregnancy after preimplantation genetic diagnosis by fluorescence in situ hybridization using 18-, X-, and Y-chromosome probes in an infertile male with mosaic trisomy 18 // J. Assist. Reprod. and Genet., 2000. Vol. 17, N 4.-С.229
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