PubRank

L Badía

Author PubWeight™ 4.68‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain. Clin Genet 1999 0.81
2 Pediatric brain tumors: loss of heterozygosity at 17p and TP53 gene mutations. Cancer Genet Cytogenet 1998 0.79
3 Nucleolus organizer regions (NORs) inserted in 6q15. Hum Genet 1989 0.78
4 X-linked dysmorphic syndrome with mental retardation. Clin Genet 1987 0.77
5 A novel TP53 germ-line mutation identified in a girl with a primitive neuroectodermal tumor and her father. Cancer Genet Cytogenet 1998 0.77
6 Translocation (11;22) in Ewing's sarcoma. Cancer Genet Cytogenet 1985 0.76
7 Refractory anemia with monosomy 2 and a double minute chromosome. Cancer Genet Cytogenet 1987 0.75
8 Recombinant X chromosome in a prenatal diagnosis. Cytogenet Genome Res 2006 0.75
9 Trisomy 4: another specific anomaly in acute nonlymphocytic leukemia. Cancer Genet Cytogenet 1987 0.75
10 [Importance of cytogenetics in the study of acute non-lymphoblastic leukemias]. Sangre (Barc) 1991 0.75
11 [Chromosomal heteromorphism in patients with chronic lymphocytic leukaemia (author's transl)]. Sangre (Barc) 1977 0.75
12 Trisomy of the long arm of chromosome 1 in patients with hematologic malignancies and solid tumors: report of six cases. Cancer Genet Cytogenet 1988 0.75
13 A fragile X family with high penetrance in females: risk heterogeneity? Clin Genet 1992 0.75
14 Pericentric inversions of chromosome 12 in two families. Hum Genet 1981 0.75
15 [Cytogenetics and hematology]. Med Clin (Barc) 1983 0.75
16 [Familial chronic jaundice caused by nonspherocytic hemolytic anemia, with increase of erythrocyte pyruvate kinase]. Rev Clin Esp 1971 0.75
17 [Down's syndrome and leukemia]. Med Clin (Barc) 1986 0.75
18 Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features. Clin Genet 2001 0.75
19 Chromosome 11 abnormalities in myelodysplastic syndromes. Cancer Genet Cytogenet 1999 0.75
20 [Genetic analysis of Friedreich's ataxia using polymorphic DNA markers]. Med Clin (Barc) 1990 0.75
21 [Chromosomic identification in Robertsonian translocations by a banding technic]. Sangre (Barc) 1973 0.75
22 [Cytogenetics in the acute leukemias]. Sangre (Barc) 1981 0.75
23 [Cytogenetics in the study of myelodysplastic syndromes]. Sangre (Barc) 1985 0.75