Benet i Català, Jordi
Jordi Benet
VIAF ID: 86651018 ( Personal )
Permalink: http://viaf.org/viaf/86651018
Preferred Forms
-
- 100 1 0 ‡a Benet i Català, Jordi
- 100 1 _ ‡a Benet i Català, Jordi
- 100 0 _ ‡a Jordi Benet
4xx's: Alternate Name Forms (7)
Works
Title | Sources |
---|---|
Anàlisi citogenètica de l'espermatozoide d'homes normals | |
Aneuploid and unbalanced sperm in two translocation carriers : evaluation of the genetic risk | |
Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes | |
Caracterización múltiple de la fragmentación del ADN espermático en pacientes infértiles | |
Chromosome aberrations in human spermatozoa treated with Ca2+ ionophore A23187 | |
Chromosome abnormalities in human spermatozoa after albumin or TEST-Yolk capacitation | |
Crossover frequency and synaptonemal complex length : their variability and effects on human male meiosis | |
Cytogenetic studies in motile sperm from normal men | |
Diagnóstico preconcepcional | |
Efecte de la fragmentació de cadena senzilla i doble del DNA espermàtic en la fertilitat masculina | |
Estudi cromosòmic del espermatozoide humà | |
Estudio de variantes estructurales del genoma humano asociadas a trastornos del neurodesarrollo | |
Expression of a possible constitutional "hot spot" in sperm chromosomes of a patient treated for Wilms̀ tumor | |
Expression of fragile sites in human sperm and lymphocyte chromosomes | |
FISH characterization of a dicentric Yq(p11.32) isochromosome in an azoospermic male | |
From spermatocytes to sperm : meiotic behaviour of human male reciprocal translocations | |
Genetics of human spermatozoa | |
Hamster origin of metaphases with multiple chromosome rearrangements in first cleavage human-hamster embryos | |
Human sperm chromosomes : long-term effect of cancer treatment | |
Hypomethylation of human sperm pronuclear chromosomes | |
The Importance of aneuploidy screening in reciprocal translocation carriers | |
Improvement of sperm quality in abnormal semen samples using a modified swim-up procedure | |
Karyotyping of human synaptonemal complexes by cenM-FISH | |
Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36) | |
Meiotic chromosome studies and synaptonemal complex analyses by light and electron microscopy in 47 infertile or sterile males | |
Meiotic segregation analysis in a t(4;8) carrier : comparison of FISH methods on sperm chromosome metaphases and interphase sperm nuclei | |
El Modelo animal como complemento al programa de FIV en humanos | |
A New synaptic anomaly : irregular synaptonemal complexes | |
PGD in female carriers of balanced Robertsonian and reciprocal translocations by first polar body analysis | |
Portadores de reorganizaciones cromosómicas: segregación meiótica en espermatogénesis y consecuencias | |
Preimplantation genetic screening and human implantation | |
Problemes de genètica humana : 1r curs de medicina | |
Re, Pellestor et al. on sperm chromosomes | |
Reliability of comparative genomic hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes | |
Segregation analysis in a man heterozygous for a pericentric inversion of chromosome 7 (p13;q36) by sperm chromosome studies | |
Significance of structural chromosome aberrations in human sperm : analysis of induced aberrations | |
Sperm chromosome studies in an infertile man with partial, complete asynapsis of meiotic bivalents | |
Sperm chromosome studies in individuals treated for testicular cancer | |
Sperm segregation analysis of a complex chromosome rearrangement, 2;22;11, by whole chromosome painting | |
Study of human sperm chromosomes by sequential transmission and scanning electron microscopy | |
Synapsis and meiotic recombination analyses : MLH1 focus in the XY pair as an indicator | |
The Use of a cell-cycle phase-marker may decrease the percentage of errors when using FISH in PGD | |
Validació de l'anàlisi citogenètica exhaustiva de tot el complement cromosòmic en cèl·lula única : aplicació translacional al Diagnòstic Genètic Preimplantacional per factor masculí | |
XY-trivalent association and synaptic anomalies in a male carrier of a Robertsonian t(13 ;14) translocation |