C. Fuster

发表

X chromosome dosage by quantitative fluorescent PCR and rapid prenatal diagnosis of sex chromosome aneuploidies.

V. Cirigliano, M. Ejarque, C. Fuster, 2002, Molecular human reproduction.

Bends in human mitotic metaphase chromosomes revisited: 15q11-13 is the most frequent non-random autosomal bend in blood cultures.

C. Fuster, R. Miró, A. Plaja, 2001, American journal of medical genetics.

Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR. Assessment on 18,000 consecutive clinical samples.

G. Voglino, V. Cirigliano, M. Ejarque, 2004, Molecular human reproduction.

Chromosome abnormalities in peripheral blood lymphocytes from untreated Hodgkin's patients

G. Berrozpe, C. Fuster, M. Caballín, 1988, Human Genetics.

Heterochromatin decondensation in chromosomes from chorionic villus samples

C. Fuster, R. Miró, J. Egozcue, 1991, Prenatal diagnosis.

Characterization of a de novo complex chromosomal rearrangement in a patient with cri‐du‐chat and trisomy 5p syndromes

C. Fuster, E. Guillén-Navarro, M. Ballesta-Martínez, 2009, American journal of medical genetics. Part A.

Chromosomal instability in amniocytes from fetuses of mothers who smoke.

C. Fuster, J. Egozcue, R. A. de la Chica, 2005, JAMA.

Fragile sites and breakpoints in constitutional rearrangements and in human sperm chromosomes

C. Fuster, L. Barrios, J. Egozcue, 1989, Human Genetics.

Expression of folate-sensitive fragile sites in lymphocyte chromosomes

C. Fuster, L. Barrios, J. Egozcue, 1989, Human Genetics.

Expression of fragile sites in human sperm and lymphocyte chromosomes

C. Fuster, J. Egozcue, J. Navarro, 1989, Human Genetics.

Analysis of kidney tumors by comparative genomic hybridization and conventional cytogenetics.

C. Fuster, M. Caballín, C. Casadevall, 2002, Cancer genetics and cytogenetics.

Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity.

R. Happle, C. Fuster, E. Geán, 2009, Archives of dermatology.

A comparative genomic hybridization study in a 46,XX male.

C. Fuster, J. Egozcue, M. Carrera, 2002, Fertility and sterility.

Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis

C. Fuster, M. Carrera, R. Baraibar, 2002, Prenatal diagnosis.

Chromosomal instability in breast cancer patients

C. Fuster, M. Caballín, L. Barrios, 1991, Human Genetics.

Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24.

C. Fuster, A. Plaja, E. Sarret, 2004, Fertility and sterility.

Human supernumeraries: are they B chromosomes?

C. Fuster, J. Egozcue, M. Rigola, 2004, Cytogenetic and Genome Research.

What Are B Chromosomes

C. Fuster, J. Egozcue, M. Rigola, 2004 .

Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations

C. Fuster, T. Vendrell, M. M. Pérez, 2002, Journal of medical genetics.

Familial complex chromosome rearrangement ascertained by in situ hybridisation.

C. Fuster, J. Egozcue, L. Míguez, 1997, Journal of medical genetics.

Heterogeneity of a Constitutional Complex Chromosomal Rearrangement in 2q

C. Fuster, M. Milá, Mónica Santos, 2016, Cytogenetic and Genome Research.

Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin.

C. Fuster, E. Guillén-Navarro, J. A. Bafallíu, 2006, European journal of medical genetics.

Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.

A. Dufke, K. Mrasek, T. Liehr, 2008, International journal of molecular medicine.

Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.

K. Mrasek, T. Liehr, C. Fuster, 2007, Fertility and Sterility.

Rapid prenatal diagnosis of common chromosome aneuploidies by QF‐PCR, results of 9 years of clinical experience

G. Voglino, V. Cirigliano, M. Ejarque, 2009, Prenatal diagnosis.

Rapid Prenatal Diagnosis by QF‐PCR: Evaluation of 30,000 Consecutive Clinical Samples and Future Applications

G. Voglino, V. Cirigliano, C. Fuster, 2006, Annals of the New York Academy of Sciences.

Assessment of new markers for the rapid detection of aneuploidies by quantitative fluorescent PCR (QF-PCR).

V. Cirigliano, C. Fuster, M. Adinolfi, 2001, Annals of human genetics.

Chromosome inversions involved in the chromosome evolution of the Hominidae and in human constitutional chromosome abnormalities

C. Fuster, M. Caballín, J. Egozcue, 1992 .

Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies.

V. Cirigliano, M. Ejarque, C. Fuster, 2001, Molecular human reproduction.

Cytogenetic effects of radiotherapy. Breakpoint distribution in induced chromosome aberrations.

C. Fuster, M. Caballín, L. Barrios, 1989, Cancer genetics and cytogenetics.

A 11.7-Mb Paracentric Inversion in Chromosome 1q Detected in Prenatal Diagnosis Associated with Familial Intellectual Disability

N. Baena, C. Fuster, V. Catalá, 2015, Cytogenetic and Genome Research.

Identification of two de novo partial trisomies by comparative genomic hybridization

C. Fuster, J. Egozcue, M. Carrera, 2001, Clinical genetics.

Cytogenetic effects of radiotherapy: frequency and types of chromosome aberrations.

C. Fuster, M. Caballín, L. Barrios, 1990, International journal of radiation oncology, biology, physics.

Lymphocyte and sperm chromosome studies in cancer-treated men

X. Bonfill, C. Fuster, M. Caballín, 1990, Human Genetics.

Chromosomal fragile site 1q21 in schizophrenic patients.

R. Guillamat, L. Fañanás, C. Fuster, 1997, The American journal of psychiatry.

Spontaneous chromosome fragility in chorionic villus cells.

C. Fuster, J. Egozcue, M. M. Pérez, 1991, Early human development.

Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis.

C. Fuster, A. Plaja, J. Egozcue, 2001, American journal of medical genetics.

Chromosome instability in bladder carcinoma patients.

C. Fuster, M. Caballín, L. Barrios, 1989, Cancer genetics and cytogenetics.

Telomere association of chromosomes induced by aphidicolin in a normal individual

C. Fuster, L. Barrios, J. Egozcue, 1990, Human Genetics.

Intrachromosomal partial triplication of chromosome 13 secondary to a paternal duplication with mild phenotypic effect

C. Fuster, Mónica Santos, E. Guillén-Navarro, 2008, American journal of medical genetics. Part A.

Sequential and combined G-banding for identifying breakpoints in sister chromatid exchanges.

C. Fuster, L. Barrios, J. Egozcue, 1992, Biotechnic & histochemistry : official publication of the Biological Stain Commission.

Fragile sites, chromosome evolution, and human neoplasia

C. Fuster, J. Egozcue, José Egozcue, 1987, Human Genetics.

Evaluation of Sample Stability and Automated DNA Extraction for Fetal Sex Determination Using Cell-Free Fetal DNA in Maternal Plasma

V. Cirigliano, C. Fuster, M. Cañadas, 2013, BioMed research international.

Development and Validation of Multiplex Real-Time PCR Assay for Noninvasive Prenatal Assessment of Fetal RhD Status and Fetal Sex in Maternal Plasma

V. Cirigliano, C. Fuster, M. Cañadas, 2013, Fetal Diagnosis and Therapy.

Comparative genomic hybridization analysis of transitional cell carcinomas of the renal pelvis.

C. Fuster, M. Caballín, C. Casadevall, 2001, Cancer genetics and cytogenetics.

Ectopic nucleolus organizer regions in a patient with premature ovarian failure.

C. Fuster, A. Plaja, E. Lloveras, 2006, Fertility and sterility.

Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR: large scale clinical application and future implications

G. Voglino, V. Cirigliano, C. Fuster, 2008 .

Concurrence of the triple-X syndrome and expression of the fragile site Xq27.3

C. Fuster, L. Barrios, J. Egozcue, 1988, Human Genetics.

Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations

K. Mrasek, T. Liehr, C. Fuster, 2010, American journal of medical genetics. Part A.

Assessment of new markers for the rapid detection of aneuploidies by quantitative fluorescent PCR (QF–PCR)

V. Cirigliano, C. Fuster, M. Adinolfi, 2001 .

Rapid prenatal diagnosis of aneuploidies

V. Cirigliano, M. Ejarque, C. Fuster, 2002, The Lancet.

Can sister chromatid intercrossings be considered as prelesions?

C. Fuster, L. Barrios, J. Egozcue, 1988, Human Genetics.