Published in Am J Med Genet on April 01, 1992
New lethal acrofacial dysostosis syndrome. Am J Med Genet (1991) 1.70
Correlation of E-cadherin expression with differentiation grade and histological type in breast carcinoma. Am J Pathol (1993) 2.74
New acrofacial dysostosis syndrome in 3 sibs. Am J Med Genet (1990) 2.63
p53 protein expression in viral warts from patients with epidermodysplasia verruciformis. Br J Dermatol (1995) 2.04
Immune responsiveness and lymphokine production in patients with tuberculosis and healthy controls. Infect Immun (1994) 1.73
Characterization of the A673 cell line (Ewing tumor) by molecular cytogenetic techniques. Cancer Genet Cytogenet (2003) 1.70
Changes in the long bones due to fetal immobility caused by neuromuscular disease. A radiographic and histological study. J Bone Joint Surg Am (1988) 1.64
beta-catenin expression pattern in stage I and II ovarian carcinomas : relationship with beta-catenin gene mutations, clinicopathological features, and clinical outcome. Am J Pathol (1999) 1.55
Strong constraints on the rare decays B(s)(0) → μ+ μ- and B0 → μ+ μ-. Phys Rev Lett (2012) 1.50
Clinical course, treatment, and multivariate analysis of risk factors for pyogenic liver abscess. Am J Surg (2001) 1.50
First observation of the decays B(0) → D(+)K(-)π(+)π(-) and B(-) → D(0)K(-)π(+)π(-). Phys Rev Lett (2012) 1.50
561del4 defines a novel small deletion hotspot in the interferon-gamma receptor 1 chain. Clin Immunol (2002) 1.43
Fluorescence in situ hybridization study of TEL/AML1 fusion and other abnormalities involving TEL and AML1 genes. Correlation with cytogenetic findings and prognostic value in children with acute lymphocytic leukemia. Haematologica (2001) 1.41
Skeletal changes in fetal akinesia. Pediatr Radiol (1989) 1.38
Effects of immobilization on fetal bone development. A morphometric study in newborns with congenital neuromuscular diseases with intrauterine onset. Calcif Tissue Int (1988) 1.33
Distinct genomic aberration patterns are found in familial breast cancer associated with different immunohistochemical subtypes. Oncogene (2007) 1.28
Molecular profiling of docetaxel cytotoxicity in breast cancer cells: uncoupling of aberrant mitosis and apoptosis. Oncogene (2006) 1.25
Microsatellite instability, MLH-1 promoter hypermethylation, and frameshift mutations at coding mononucleotide repeat microsatellites in ovarian tumors. Cancer (2001) 1.24
beta-Catenin expression pattern, beta-catenin gene mutations, and microsatellite instability in endometrioid ovarian carcinomas and synchronous endometrial carcinomas. Diagn Mol Pathol (2001) 1.20
Severe axial anomalies in the oculo-auriculo-vertebral (Goldenhar) complex. Am J Med Genet (1993) 1.19
MLH1 germline epimutations in selected patients with early-onset non-polyposis colorectal cancer. Clin Genet (2007) 1.17
beta-catenin expression in pilomatrixomas. Relationship with beta-catenin gene mutations and comparison with beta-catenin expression in normal hair follicles. Br J Dermatol (2001) 1.15
The genomic profile of HER2-amplified breast cancers: the influence of ER status. J Pathol (2008) 1.14
Combined effect of bacteriocins on the survival of various Listeria species in broth and meat system. Curr Microbiol (2000) 1.14
Endometrial carcinoma: molecular alterations involved in tumor development and progression. Oncogene (2012) 1.14
Molecular profiling pleomorphic lobular carcinomas of the breast: evidence for a common molecular genetic pathway with classic lobular carcinomas. J Pathol (2008) 1.13
Electrophysiologic studies in atrial fibrillation. Slow conduction of premature impulses: a possible manifestation of the background for reentry. Am J Cardiol (1983) 1.13
Immunological capabilities of patients with atopic dermatitis. J Invest Dermatol (1966) 1.11
Lhermitte-Duclos disease and Cowden disease: clinical and genetic study in five patients with Lhermitte-Duclos disease and literature review. Acta Neurochir (Wien) (2004) 1.10
An unusual variant of chromosome 16. Two new cases. Hum Genet (1988) 1.09
Chromosomal changes pattern and gene amplification in T cell non-Hodgkin's lymphomas. Leukemia (2001) 1.08
[Achondroplasia: molecular study of 28 patients]. Med Clin (Barc) (1998) 1.06
Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly. Am J Med Genet (1993) 1.05
Pathology and gene expression of hereditary breast tumors associated with BRCA1, BRCA2 and CHEK2 gene mutations. Oncogene (2006) 1.04
Nucleotide sequence and organization of an H2-uptake gene cluster from Rhizobium leguminosarum bv. viciae containing a rubredoxin-like gene and four additional open reading frames. J Mol Biol (1992) 1.03
A haplotype containing the p53 polymorphisms Ins16bp and Arg72Pro modifies cancer risk in BRCA2 mutation carriers. Hum Mutat (2006) 1.02
Adrenal gland leiomyoma in a child with acquired immunodeficiency syndrome. Pediatr Pathol Lab Med (1996) 1.01
Mitochondrial activity, distribution and segregation in bovine oocytes and in embryos produced in vitro. Reprod Domest Anim (2006) 0.97
Personalized cancer medicine and the future of pathology. Virchows Arch (2011) 0.97
JunD is involved in the antiproliferative effect of Delta9-tetrahydrocannabinol on human breast cancer cells. Oncogene (2008) 0.95
Proton permeability induced by polyene antibiotics. A plausible mechanism for their inhibition of maltose fermentation in yeast. FEBS Lett (1978) 0.95
Comparative finite element analysis of the debonding process in different concepts of cemented hip implants. Ann Biomed Eng (2010) 0.95
Multivacuolated cells in human cartilage canals. Acta Anat (Basel) (1985) 0.94
Methimazole in animal feed and congenital aplasia cutis. Lancet (1992) 0.94
Prenatal growth of the human mandibular condylar cartilage. Am J Orthod Dentofacial Orthop (1995) 0.94
Postsurgical focal testicular infarct. Urol Int (1986) 0.92
Value of clinical analysis in epidemiological research: the Spanish registry experience. Am J Med Genet (1991) 0.92
Expression pattern of the cell adhesion molecules. E-cadherin, P-cadherin and alpha 6 beta 4 intergrin is altered in pre-malignant skin tumors of p53-deficient mice. Int J Cancer (1996) 0.92
Fragmented electrograms and continuous electrical activity in atrial flutter. Am J Cardiol (1986) 0.92
Mulibrey nanism: three additional patients and a review of 39 patients. Am J Med Genet (1995) 0.91
Lethal Pallister-Killian syndrome: phenotypic similarity with Fryns syndrome. Am J Med Genet (1994) 0.91
The new truncated somatostatin receptor variant sst5TMD4 is associated to poor prognosis in breast cancer and increases malignancy in MCF-7 cells. Oncogene (2011) 0.91
Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study. Ann Oncol (2010) 0.90
De novo interstitial deletion q16.2q21 on chromosome 6. Am J Med Genet (1995) 0.90
The prognostic significance of P-cadherin in infiltrating ductal breast carcinoma. Mod Pathol (2001) 0.90
Goya's artwork imaging with Terahertz waves. Opt Express (2013) 0.89
High frequency of beta-catenin mutations in borderline endometrioid tumours of the ovary. J Pathol (2006) 0.89
Structure functional expression and spatial distribution of a cloned cDNA encoding a rat 5-HT1D-like receptor. J Recept Res (1993) 0.88
Acute hemorrhagic conjunctivitis epidemic in Colon, Republic of Panama. Am J Epidemiol (1986) 0.88
E-cadherin expression in basal cell carcinoma. Br J Cancer (1994) 0.88
Atrial flutter mapping and ablation. I. Studying atrial flutter mechanisms by mapping and entrainment. Pacing Clin Electrophysiol (1996) 0.88
Inhibition of virulent Mycobacterium tuberculosis by Bcg(r) and Bcg(s) macrophages correlates with nitric oxide production. J Infect Dis (1997) 0.88
Changes in young rat radius following excision of the perichondrial ring. Calcif Tissue Int (1985) 0.87
Beta-catenin expression pattern in small cell lung cancer: correlation with clinical and evolutive features. Histol Histopathol (2001) 0.86
Mechanisms of entrainment of human common flutter studied with multiple endocardial recordings. Circulation (1994) 0.85
Lethal short rib-polydactyly syndromes: further evidence for their overlapping in a continuous spectrum. J Med Genet (1993) 0.85
Neuroepithelial cyst in the optic nerve. Case report. J Neurosurg (1987) 0.84
DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas. Br J Cancer (2013) 0.84
beta-catenin expression pattern in primary oesophageal squamous cell carcinoma. Relationship with clinicopathologic features and clinical outcome. Virchows Arch (2000) 0.84
Prevention of hyperacute rejection in a model of orthotopic liver xenotransplantation from pig to baboon using polytransgenic pig livers (CD55, CD59, and H-transferase). Transplant Proc (2005) 0.84
Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients. Breast Cancer Res Treat (2014) 0.84
Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies. Am J Med Genet (1993) 0.84
Loss of heterozygosity in BRCA1 and BRCA2 markers and high-grade malignancy in breast cancer. Breast Cancer Res Treat (1999) 0.84
Tetra-phocomelia with multiple malformations: X-linked amelia, or Roberts syndrome, or DK-phocomelia syndrome? Am J Med Genet (1992) 0.84
Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion. Acta Neuropathol (2004) 0.83
Intra-uterine long bone growth in small-for-gestational-age infants. Eur J Pediatr (1992) 0.83
Morphological changes in long bone development in fetal akinesia deformation sequence: an experimental study in curarized rat fetuses. Teratology (1992) 0.83
Malignant rhabdoid tumor of the tongue. A case report with immunohistochemical and ultrastructural findings. Oral Surg Oral Med Oral Pathol (1988) 0.83
Verrucous carcinoma of the skin associated with syringadenoma papilliferum: a case report. J Cutan Pathol (1987) 0.82
Mechanisms underlying trypanosome-elicited immunosuppression. Ann Soc Belg Med Trop (1992) 0.82
Proximal partial 5p trisomy resulting from a maternal (19;5) insertion. Am J Med Genet (1997) 0.82
A new case of fibrochondrogenesis from Spain. J Med Genet (1996) 0.82
Epidemiological analysis of the schisis association in the Spanish registry of congenital malformations. Am J Med Genet (1997) 0.81
Continuous renal replacement therapy in neonates and young infants during extracorporeal membrane oxygenation. Int J Artif Organs (2007) 0.81
Chromosome 4p16 and osteochondroplasias. Nat Genet (1994) 0.81
Primary midline developmental field. II. Clinical/epidemiological analysis of alteration of laterality (normal body symmetry and asymmetry). Am J Med Genet (1995) 0.81
Segmentation anomalies of the vertebras and ribs: a developmental field defect: epidemiologic evidence. Am J Med Genet (1994) 0.81
New case of limb body-wall complex associated with sirenomelia sequence. Am J Med Genet (1992) 0.81
Craniorachischisis totalis and sirenomelia. Am J Med Genet (1992) 0.81
Sirenomelia and anencephaly. Am J Med Genet (1991) 0.81
Osteochondroma induced by reflection of the perichondrial ring in young rat radii. Calcif Tissue Int (1987) 0.81
Radiocesium accumulation in edible wild mushrooms from coniferous forests around the Nuclear Centre of Mexico. Sci Total Environ (1998) 0.80
Signet-ring stromal tumor of the ovary: a histochemical, immunohistochemical and ultrastructural study. Virchows Arch A Pathol Anat Histopathol (1993) 0.80