J. Benítez

发表

Chromosomal patterns in human malignant astrocytomas.

J. Rey, M. Bello, J. M. de Campos, 1987, Cancer genetics and cytogenetics.

Cytogenetic findings in an effusion secondary from pleural mesothelioma.

J. Rey, M. Bello, M. Avilés, 1987, Cancer genetics and cytogenetics.

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q

P. Humphries, C. Ayuso, P. Kenna, 1993, Nature Genetics.

Parental origin of chromosomal non‐disjunction in a 49,XXXXY male using recombinant‐DNA techniques

C. Ayuso, E. Fernández, M. Villamar, 1989, Clinical genetics.

Δ F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families

X. Estivill, P. Gasparini, B. Dallapiccola, 1990, Prenatal diagnosis.

C-banding studies in lymphocytes from patients with tumors of the nervous system.

J. Rey, J. M. de Campos, J. Benítez, 1985, Cancer genetics and cytogenetics.

Frequency of constitutional chromosome alterations in patients with hematologic neoplasias.

C. Ayuso, C. Ramos, J. Benítez, 1987, Cancer genetics and cytogenetics.

Frequent retinoic acid receptor alpha (Rar‐α) gene rearrangements and no point mutations of N‐Ras gene in fifteen cases of acute promyelocytic leukemia

M. Robledo, E. Arranz, A. Santón, 1994, American journal of hematology.

Translocation of a supernumerary Y to a 15: Study of six cases (three males and three females) in three generations

C. Ramos, J. Benítez, A. Sánchez-Cascos, 1979, Human Genetics.

Two fertile Turner women in a family

M. C. Ayuso, J. Benítez, A. Sánchez-Cascos, 1984, Clinical genetics.

Chromosome studies in two human brain tumors.

J. Rey, M. Bello, J. M. de Campos, 1983, Cancer genetics and cytogenetics.

Serial cytogenetic study of a human glioma cell line.

J. Rey, M. Bello, C. Ramos, 1983, Cancer genetics and cytogenetics.

Acute nonlymphocytic leukemia with severe hypodiploidy and one double minute chromosome.

J. Rey, M. Bello, J. Benítez, 1985, Cancer genetics and cytogenetics.

Deletion 3p in two lung adenocarcinomas metastatic to the brain.

J. Rey, M. Bello, J. M. de Campos, 1987, Cancer genetics and cytogenetics.

Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity

I. Gut, B. Wirth, F. Muntoni, 2020, The Journal of molecular diagnostics : JMD.

Cytogenetic findings in a human malignant melanoma metastatic to the brain.

J. Rey, M. Bello, J. M. de Campos, 1985, Cancer genetics and cytogenetics.

Chromosome banding patterns in patients with chronic myelocytic leukemia.

F. Prieto, F. Carbonell, J. Sánchez-Fayos, 1982, Cancer genetics and cytogenetics.

Homozygosity for a Robertsonian translocation (13q14q) in three offspring of heterozygous parents.

J. Rey, P. Martínez-Castro, J. Benítez, 1984, Cytogenetics and cell genetics.

A case of pituitary adenoma with 58 chromosomes.

J. Rey, M. Bello, J. M. de Campos, 1986, Cancer genetics and cytogenetics.

Somatic stability in chorionic villi samples and other Huntington fetal tissues

B. Brambati, C. Ayuso, M. Robledo, 1995, Human Genetics.

Crossover in a Spanish cystic fibrosis family

E. Fernández, M. Villamar, J. Benítez, 1990, Human Genetics.

Autosomal dominant retinitis pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locus.

P. Humphries, C. Ayuso, P. Kenna, 1992, Human molecular genetics.

Karyotypic evolution in patients with myelodysplastic syndromes.

H. Heimpel, F. Carbonell, J. Benítez, 1985, Cancer genetics and cytogenetics.

Ring chromosome 6: clinical and cytogenetic behaviour.

C. Ayuso, C. Paz-y-Miño, J. Benítez, 1990, American journal of medical genetics.

Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families

M. Bayés, M. Baiget, D. Grinberg, 1995, Human Genetics.

Homozygous tandem duplication within the gene encoding the β‐subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa

M. Bayés, S. Amselem, M. Baiget, 1995 .

Homozygous myotonic dystrophy: clinical and molecular studies of three unrelated cases.

J. Rosell, M. Baiget, I. Illa, 1996 .

Homozygous myotonic dystrophy: clinical and molecular studies of three unrelated cases

J. Rosell, M. Baiget, I. Illa, 1996, Neuromuscular Disorders.

cases . and molecular studies of three unrelated Homozygous myotonic dystrophy : clinical

J. Rosell, M. Baiget, I. Illa, 2022 .

Novel rhodopsin mutation in an autosomal dominant retinitis pigmentosa family: phenotypic variation in both heterozygote and homozygote Val137Met mutant patients

C. Ayuso, M. Robledo, C. Ramos, 1996, Human Genetics.

Recurrence of Down syndrome associated with microchromosome

C. Ramos, J. Benítez, A. Sánchez-Cascos, 1979, Human Genetics.

Cytogenetic clones in a recurrent neurofibroma.

J. Rey, M. Bello, J. Sarasa, 1987, Cancer genetics and cytogenetics.

A point mutation changes the polymorphisms pattern in a cystic fibrosis carrier family

E. Fernández, A. Santón, J. Benítez, 1992, Human Genetics.

Trinucleotide (CAG) repeat expansion in chromosomes of Spanish patients with Huntington's disease

E. Fernández, M. Robledo, C. Ramos, 1994, Human Genetics.

Cytogenetic studies in 18 patients with secondary blood disorders.

F. Prieto, F. Carbonell, J. Benítez, 1986, Cancer genetics and cytogenetics.

bcr breakpoint location in Spanish patients with chronic myelogenous leukemia.

A. Valiente, E. Prieto, J. Benítez, 1992, Cancer genetics and cytogenetics.

Ph-positive chronic myeloid leukemia in a child. Rearrangement of the breakpoint cluster region.

A. Valiente, J. Benítez, M. Bernácer, 1990, Cancer genetics and cytogenetics.

Leukemic transformation in patients with the 5q- alteration: analysis of the behavior of the 5q- clones in preleukemic to leukemic phases.

C. Ramos, C. Toledo, J. Benítez, 1987, Cancer genetics and cytogenetics.

C-band pattern in patients with nervous system tumors.

J. Rey, M. Bello, M. Kusak, 1987, Cancer genetics and cytogenetics.