Biomedical - Orthopedic surgery and traumatology
Principal researcher: Dr. F. Vidal Domínguez, School of Science, Universitat Autònoma de Barcelona.
- Year:
- 1994
- Derived publications:
- Vidal F, Blanco J and Egozcue J. Detección de aneuploidías en espermatozoides humanos. Progresos en Diagnóstico Prenatal, 1995, 7: 472-474.
- Vidal F, Blanco J, Egozcue J. No-disyunción y estudio de gametos. SD-DS International Medical Review on Down Syndrome, 1997, 1: 8.
- Blanco J, Egozcue J and Vidal F. Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hibridization. Human Genetics, 1996, 11: 722-726.
- Blanco J, Egozcue J and Vidal F. Increased Incidence of disomic sperm nuclei in a 47, XYY male assessed by fluorescent in situ hybridization (FISH). Hum Genet, 1997, 99: 413-416.
- Colls P, Blanco J, Martínez-Pasarell O, Egozcue J, Vidal F, Guitart M and Templado C. Chromosome segregation in a man heterozygous for a pericentric inversion, inv (9)(p11q13), analysed by using sperm karyotyping and two-colour fluorescence in situ hybridization on sperm nuclei. Hum Genet, 1997, 99: 761-765.
- Blanco J, Colls P, Templado C, Egozcue J, Vidal F. Structural abnormalities and lack of an interchromosomal effect for chromosome 21: a FISH study in spermatozo. Cytogenet Cell Genet 1997; 77 (suppl. 1): 10.
- Blanco J, Egozcue J, Clusellas N, Vidal F. FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: results in a translocation carrier, t(5;8)(q33;q13). Cytogenet Cell Genet 1998, 83: 275-280.
- Blanco J, Egozcue J, Vidal F. Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridization. Hum Reprod, 1996, 11: 722-726.
- Blanco J, Egozcue J, Vidal F. Non-disjunction of chromosome 21 in human spermatozoa: a FISH study in a high risk population. J Assist Reprod Genet, 1997, 14 (8): 426.
- Blanco J, Gabau E, Gómez D, Baena N, Guitart M, Egozcue J, Vidal F. Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome: increased incidence in cases of paternal origin. Am J Hum Genet 1998, 63: 1067-1072.
- Blanco J, Rubio MC, Simón C, Egozcue J, Vidal F. A fluorescent in-situ hybridization study of the spermatogenic process and sperm production in a 47,XYY and a 47,XXY/46, XY infertile males: implications for ICSI. Human Reproduction, 1996, 11: 159-160.
- Blanco J, Egozcue J and Vidal F. Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hibridization. Human Genetics, 1996, 11: 722-726.
- Blanco J, Simón C, Rubio C, Egozcue J, Vidal F. Incidence of disomic sperm nuclei in a 47, XYY male assessed by fluorescent in-situ hybridization (FISH). European Journal of Human Genetics, 1996, 4 (suppl 1): 40.
- Egozcue J, Blanco J, Vidal F. Chromosome studies in human sperm nuclei using fluorescence in situ hybridization (FISH). Human Reproduction Update 1997, 3: 441-452.
- Valero R, Bayés M, Francisca Sánchez-Font, González-Ángulo O, Gónzález-Duarte R, Marfany G. Characterization of alternatively spliced products and tissue-specific isoforms of USP28 and USP25. Genome Biol, 2001.
- Vidal F, Blanco J, Egozcue J. Nondisjunction gamete studies. Cytogenetics and Cell Genetics, 1997, 77 (suppl. 1): 4.
- Vidal F, Fugger EF, Blanco J, Keyvanfar K, Català V, Norton M, Hazelrigg WB, Black SH, Levinson G, Egozcue J, Schulman JD. Efficiency of MicroSort flow cytometry for producing sperm populations enriched in X- or Y-chromosome haplotypes: a blind trial assessed by double and triple colour fluorescent in-situ hybridization. Hum Reprod, 1998, 13: 308-312.
- Vidal M, Blanco J, Egozcue J. Detección de aneuploidías en espermatozoides humanos. Progresos en Diagnóstico Prenatal, 1995, 7: 472-474.