Published in Hum Genet on March 01, 1986
Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes. Cell (2009) 2.52
Chromosomal instability and cytoskeletal defects in oral cancer cells. Proc Natl Acad Sci U S A (2000) 1.60
Centromere activity in dicentric small supernumerary marker chromosomes. Chromosome Res (2010) 0.96
Engineered human dicentric chromosomes show centromere plasticity. Chromosome Res (2005) 0.90
Aneuploidy and chromosomal instability: a vicious cycle driving cellular evolution and cancer genome chaos. Cancer Metastasis Rev (2013) 0.87
The role of dicentric chromosome formation and secondary centromere deletion in the evolution of myeloid malignancy. Genet Res Int (2011) 0.85
A unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies. Am J Hum Genet (1987) 0.85
Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study. J Med Genet (1998) 0.78
Not para-, not peri-, but centric inversion of chromosome 12. J Med Genet (1998) 0.77
Acentric chromosome ends are prone to fusion with functional chromosome ends through a homology-directed rearrangement. Nucleic Acids Res (2015) 0.75
Prenatal diagnosis and molecular cytogenetic analysis of a de novo isodicentric chromosome 18. Ann Saudi Med (2010) 0.75
Hospitalization costs associated with homelessness in New York City. N Engl J Med (1998) 5.90
Hospital characteristics and mortality rates. N Engl J Med (1989) 4.97
Evaluation of the HCFA model for the analysis of mortality following hospitalization. Health Serv Res (1992) 1.99
Abnormal X chromosomes in man: origin, behavior and effects. Humangenetik (1974) 1.93
Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 leads to 14qter). Am J Med Genet (1977) 1.93
X inactivation in man: a woman with t(Xq--;12q+). Am J Hum Genet (1973) 1.90
Apparently isodicentric but functionally monocentric X chromosome in man. Am J Hum Genet (1974) 1.84
Characteristics of fatal ambulance crashes in the United States: an 11-year retrospective analysis. Prehosp Emerg Care (2001) 1.64
Center for Barr body condensation on the proximal part of the human Xq: a hypothesis. Chromosoma (1974) 1.53
Association of simian immunodeficiency virus Nef with cellular serine/threonine kinases is dispensable for the development of AIDS in rhesus macaques. Nat Med (1997) 1.48
Prestige of training programs and experience of bypass surgeons as factors in adjusted patient mortality rates. Med Care (1999) 1.41
The relationship between adjusted hospital mortality and the results of peer review. Health Serv Res (1993) 1.40
Rapid development of vaccine protection in macaques by live-attenuated simian immunodeficiency virus. J Gen Virol (1996) 1.27
Cytological demonstration of mitotic crossing-over in man. Cytogenet Cell Genet (1976) 1.23
Familial bilateral renal agenesis and hereditary renal adysplasia. Z Kinderheilkd (1973) 1.22
Comparing hospitals that perform coronary artery bypass surgery: the effect of outcome measures and data sources. Am J Public Health (1994) 1.09
Localization by Q-banding of mitotic chiasmata in cases of Bloom's syndrome. Chromosoma (1976) 1.09
Psychosocial outcomes for preschool children and families after surgery for complex congenital heart disease. Pediatr Cardiol (2007) 1.08
Assessing providers of coronary revascularization: a method for peer review organizations. Am J Public Health (1992) 1.07
Spontaneous cell fusion and PCC formation in Bloom's syndrome. Chromosoma (1982) 1.07
Mortality after coronary angioplasty and coronary artery bypass surgery (the national Medicare experience). Am J Cardiol (1992) 1.06
Cytogenetics of Bloom's syndrome. Cancer Genet Cytogenet (1986) 1.06
Charges for childhood asthma by hospital characteristics. Pediatrics (1998) 1.04
A possible active segment on the inactive human X chromosome. Chromosoma (1976) 1.01
Cancers of the breast and female genital system: search for recessive genetic factors through analysis of human isolate. Am J Obstet Gynecol (1981) 1.00
Mitotic recombination and segregation of satellites in Bloom's syndrome. Chromosoma (1981) 0.98
Mitotic modifications and aberrations in cancer. Crit Rev Oncog (1989) 0.97
The XY gonadal agenesis syndrome. J Med Genet (1973) 0.97
Mitotic chiasmata, gene density, and oncogenes. Hum Genet (1985) 0.96
Pseudovaginal perineoscrotal hypospadias. Clin Genet (1972) 0.96
The phenotypic effects of small, distal Xq deletions. Hum Genet (1984) 0.95
Relaxing retinotomies and retinectomies. Surgical results and predictors of visual outcome. Arch Ophthalmol (1990) 0.95
Platynosomum fastosum in ex-captive orangutans from Indonesia. J Wildl Dis (1998) 0.95
Replication and inactivation of a dicentric X formed by telomeric fusion. Am J Obstet Gynecol (1980) 0.94
Position of the human X inactivation center on Xq. Hum Genet (1979) 0.93
The acidic region and conserved putative protein kinase C phosphorylation site in Nef are important for SIV replication in rhesus macaques. Virology (1999) 0.93
Repeated measurements of serum carotenoid, retinol and tocopherol levels in relation to colorectal cancer risk in the Women's Health Initiative. Eur J Clin Nutr (2011) 0.93
The interleukin-17 gene of herpesvirus saimiri. J Virol (1998) 0.92
Age and gender patterns in motor vehicle crash injuries: importance of type of crash and occupant role. Accid Anal Prev (2001) 0.92
Interspecies transmission of Enterozytozoon bieneusi supported by observations in laboratory animals and phylogeny. Med Microbiol Immunol (2005) 0.91
Pre-transplant identification of risk factors that adversely affect length of stay and charges for renal transplantation. Clin Transplant (1999) 0.91
X chromosome constitution and the human female phenotype. Hum Genet (1980) 0.90
Health issues for women with epilepsy: a descriptive survey to assess knowledge and awareness among healthcare providers. J Womens Health Gend Based Med (2000) 0.90
Test of the acute cardiac ischemia time-insensitive predictive instrument (ACI-TIPI) for prehospital use. Ann Emerg Med (1996) 0.89
Partial 11q trisomy syndrome. Hum Genet (1981) 0.88
Herpesvirus saimiri vFLIP provides an antiapoptotic function but is not essential for viral replication, transformation, or pathogenicity. J Virol (2000) 0.88
Hot spots and functional organization of human chromosomes. Hum Genet (1978) 0.87
Human telomeric 6; 19 translocation chromosome with a tendency to break at the fusion point. Chromosoma (1983) 0.87
Cytogenetics of fifty patients with primary amenorrhea. Am J Obstet Gynecol (1974) 0.87
Virilizing adrenal ganglioneuroma. JAMA (1978) 0.86
Increased Q fluorescence of an inactive Xq-chromosome in man. Clin Genet (1974) 0.86
Premeiotic and early meiotic stages in the pollen mother cells of Eremurus and in human embryonic oocytes. Hum Genet (1977) 0.86
Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome. J Med Genet (1975) 0.85
Mitotic chiasmata and other quadriradials in mitomycin C-treated Bloom's syndrome lymphocytes. Chromosoma (1978) 0.85
Effects of X-irradiation in G1 and G2 on Bloom's Syndrome and normal chromosomes. Hum Genet (1980) 0.85
47,XXX females, sex chromosomes, and tooth crown structure. Hum Genet (1987) 0.85
Hospitalizations for vehicle associated injuries in Wisconsin. WMJ (1999) 0.85
X chromatin, endomitoses, and mitotic abnormalities in human cervical cancer. Cancer Genet Cytogenet (1985) 0.85
Managing depression in outpatients. N Engl J Med (2001) 0.84
Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies. Fertil Steril (1983) 0.84
T-cell lymphoma caused by herpesvirus saimiri C488 independently of ie14/vsag, a viral gene with superantigen homology. J Virol (1998) 0.84
Independence of herpesvirus-induced T cell lymphoma from viral cyclin D homologue. J Exp Med (2001) 0.84
Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases. Am J Med Genet (1998) 0.84
Hormone replacement therapy in the menopause: a pro opinion. CA Cancer J Clin (1996) 0.83
What causes the abnormal phenotype in a 49,XXXXY male? Hum Genet (1987) 0.83
Chromosome breakage by 1-methyl-2-benzylhydrazine in mouse cancer cells. Cancer Res (1972) 0.83
Academic models of clinical care for women: the National Centers of Excellence in Women's Health. J Womens Health Gend Based Med (2001) 0.83
Prevention of renal allograft rejection in primates by blocking the B7/CD28 pathway. Transplantation (1999) 0.82
Are the best coronary artery bypass surgeons identified by physician surveys? Am J Public Health (1997) 0.82
Endomitosis: a reappraisal. Hum Genet (1983) 0.82
The structure and origin of giant nuclei in human cancer cells. Cancer Genet Cytogenet (1983) 0.82
The use of risk-adjusted complication rates to compare hospitals performing coronary artery bypass surgery or angioplasty. Int J Technol Assess Health Care (1992) 0.82
Mitotic crossing-over and segregation in man. Hum Genet (1981) 0.81
Cytokine gene transcription in simian immunodeficiency virus and human immunodeficiency virus-associated non-Hodgkin lymphomas. AIDS Res Hum Retroviruses (1997) 0.81
Safety and immunogenicity of ALVAC wild-type human p53 (vCP207) by the intravenous route in rhesus macaques. Vaccine (2001) 0.81
Chromosome breakage and rejoining of sister chromatids in Bloom's syndrome. Chromosoma (1979) 0.81
A boy with congenital malformations and chromosome breakage. Am J Med Genet (1980) 0.81
An anti-HIV strategy combining chemotherapy and therapeutic vaccination. J Med Primatol (1999) 0.80
Microsporidia and Candida spores: their discrimination by Calcofluor, trichrome-blue and methylene-blue combination staining. Trop Med Int Health (2000) 0.80
Assessing clinical competence of medical students in women's health care: use of the objective structured clinical examination. Obstet Gynecol (1998) 0.79
Structure and Barr body formation of an Xp + chromosome with two inactivation centers. Am J Hum Genet (1977) 0.79