Found: 29
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Filtration and recirculation of early amniotic fluid. Evaluation of cell cultures from 100 diagnostic cases.
- Published in:
- Prenatal Diagnosis, 1993, v. 13, n. 12, p. 1101, doi. 10.1002/pd.1970131205
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- Article
Transabdominal chorionic villus sampling in the second and third trimesters of pregnancy: Chromosome quality, reporting time, and feto-maternal bleeding.
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- Prenatal Diagnosis, 1993, v. 13, n. 10, p. 957, doi. 10.1002/pd.1970131010
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- Article
Cytogenetic analysis of 2928 CVS samples and 1075 amniocenteses from randomized studies.
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- Prenatal Diagnosis, 1993, v. 13, n. 8, p. 723, doi. 10.1002/pd.1970130807
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- Article
Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization.
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- Prenatal Diagnosis, 1992, v. 12, n. 4, p. 241, doi. 10.1002/pd.1970120403
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- Article
Genetic amniocentesis at 7-14 weeks of gestation.
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- Prenatal Diagnosis, 1992, v. 12, n. 4, p. 277, doi. 10.1002/pd.1970120407
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- Article
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
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- European Journal of Human Genetics, 2008, v. 16, n. 3, p. 312, doi. 10.1038/sj.ejhg.5201985
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- Article
Systematic re-examination of carriers of balanced reciprocal translocations: a strategy to search for candidate regions for common and complex diseases.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 410, doi. 10.1038/sj.ejhg.5201592
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- Article
Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences.
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- European Journal of Human Genetics, 2005, v. 13, n. 3, p. 283, doi. 10.1038/sj.ejhg.5201267
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- Article
Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA).
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- European Journal of Human Genetics, 2005, v. 13, n. 2, p. 171, doi. 10.1038/sj.ejhg.5201307
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- Article
An excess of chromosome 1 breakpoints in male infertility.
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- European Journal of Human Genetics, 2004, v. 12, n. 12, p. 993, doi. 10.1038/sj.ejhg.5201263
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- Article
High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes.
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- European Journal of Human Genetics, 2000, v. 8, n. 9, p. 661, doi. 10.1038/sj.ejhg.5200512
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- Article
High-resolution comparative genomic hybridisation yields a high detection rate of chromosomal aberrations in childhood acute lymphoblastic leukaemia.
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- European Journal of Haematology, 2003, v. 70, n. 6, p. 363, doi. 10.1034/j.1600-0609.2003.00072.x
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- Article
Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples.
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- Acta Obstetricia et Gynecologica Scandinavica, 2000, v. 79, n. 1, p. 8, doi. 10.1080/j.1600-0412.2000.079001008.x
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- Article
High-resolution comparative genomic hybridization detects extra chromosome arm 12p material in most cases of carcinoma in situ adjacent to overt germ cell tumors, but not before the invasive tumor development.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 2, p. 117, doi. 10.1002/gcc.10244
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- Article
Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 4, p. 410, doi. 10.1002/(SICI)1098-2264(199908)25:4<410::AID-GCC17>3.0.CO;2-J
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- Article
Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 144, doi. 10.1002/(SICI)1098-2264(199902)24:2<144::AID-GCC7>3.0.CO;2-9
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- Article
Detection of chromosomal aberrations in seminomatous germ cell tumours using comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 412, doi. 10.1002/(SICI)1098-2264(199712)20:4<412::AID-GCC14>3.0.CO;2-O
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- Article
Non-disjunction of chromosome 13.
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- Human Molecular Genetics, 2007, v. 16, n. 16, p. 2004, doi. 10.1093/hmg/ddm148
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- Article
Automated multiple-cell karyotyping: a clinical feasibility study.
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- Clinical Genetics, 1991, v. 39, n. 5, p. 338, doi. 10.1111/j.1399-0004.1991.tb03040.x
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- Article
Automated cytogenetic analysis: accomplishments, present status and practical future possibilities.
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- Clinical Genetics, 1989, v. 36, n. 5, p. 386, doi. 10.1111/j.1399-0004.1989.tb03217.x
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- Article
A test of a climate room for preparation of chromosome slides.
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- Clinical Genetics, 1985, v. 28, n. 3, p. 260, doi. 10.1111/j.1399-0004.1985.tb00397.x
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- Article
Automatic chromosome analysis.
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- Clinical Genetics, 1981, v. 19, n. 1, p. 26, doi. 10.1111/j.1399-0004.1981.tb00663.x
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- Article
Automatic chromosome analysis.
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- Clinical Genetics, 1980, v. 17, n. 3, p. 183, doi. 10.1111/j.1399-0004.1980.tb00131.x
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- Article
Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases.
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- Clinical Genetics, 1979, v. 16, n. 3, p. 147, doi. 10.1111/j.1399-0004.1979.tb00983.x
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- Article
Visual classification of banded human chromosomes.
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- Clinical Genetics, 1979, v. 15, n. 5, p. 430, doi. 10.1111/j.1399-0004.1979.tb01775.x
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- Article
Description of chromosome banding patterns by band transition sequences.
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- Clinical Genetics, 1979, v. 15, n. 5, p. 418, doi. 10.1111/j.1399-0004.1979.tb01774.x
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- Article
Letters to the Editor.
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- Clinical Genetics, 1976, v. 10, n. 1, p. 60, doi. 10.1111/j.1399-0004.1976.tb00010.x
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- Article
Microphotometry of banded human chromosomes III.
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- Clinical Genetics, 1976, v. 10, n. 1, p. 33, doi. 10.1111/j.1399-0004.1976.tb00006.x
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- Article
Microphotometry of banded human chromosomes II:Technique for microphotography of banding patterns.
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- Clinical Genetics, 1976, v. 9, n. 2, p. 156, doi. 10.1111/j.1399-0004.1976.tb01562.x
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- Article