Published in Prenat Diagn on August 01, 1993
Randomised controlled trial of genetic amniocentesis in 4606 low-risk women. Lancet (1986) 4.71
Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus sampling. Lancet (1997) 2.72
Care of the dying cancer patient in the emergency department: findings from a National survey of Australian emergency department clinicians. Intern Med J (2014) 2.64
Randomised comparison of amniocentesis and transabdominal and transcervical chorionic villus sampling. Lancet (1992) 2.15
[Maternal serum screening for congenital abnormalities and Down syndrome in Sønderjylland County. Eight years of experience]. Ugeskr Laeger (1999) 1.74
An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Hum Hered (1973) 1.64
Criminality in XYY and XXY men. Science (1976) 1.57
European Guidelines for Quality Assurance in Cervical Cancer Screening. Europe against cancer programme. Eur J Cancer (1993) 1.52
Larvae in the mouth. Br Dent J (2007) 1.45
Should the indications for prenatal chromosome analysis be changed? Br Med J (1977) 1.45
A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group. N Engl J Med (1992) 1.43
Biopsy of the breast. Br J Hosp Med (1981) 1.42
Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma. Genes Chromosomes Cancer (1999) 1.40
Sampling success and risk by transabdominal chorionic villus sampling, transcervical chorionic villus sampling and amniocentesis: a randomized study. Ultrasound Obstet Gynecol (1991) 1.40
Between a rock and a hard place: exploring the conflict between respecting the privacy of patients and informing their carers. Intern Med J (2009) 1.39
Cytogenetic results from the U.S. Collaborative Study on CVS. Prenat Diagn (1992) 1.35
Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man. J Med Genet (2000) 1.30
High resolution comparative genomic hybridisation in clinical cytogenetics. J Med Genet (2001) 1.29
Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals. Cytometry (1998) 1.29
Distribution of nodal metastases in nonseminomatous testis cancer. J Urol (1982) 1.29
Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY,+mar in two cases. Clin Genet (1979) 1.24
Breast self-examination: clinical results from a population-based prospective study. Br J Cancer (1984) 1.17
Comparative genomic hybridization in clinical cytogenetics. Am J Hum Genet (1995) 1.15
Choroideremia: further evidence for assignment of the locus to Xq13-Xq21. Hum Genet (1986) 1.11
Cytogenetic results of chorionic villus sampling: high success rate and diagnostic accuracy in the United States collaborative study. Am J Obstet Gynecol (1990) 1.11
Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals. Genes Chromosomes Cancer (1999) 1.11
Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother. Hum Genet (1983) 1.11
Synthesis, spectral, optical and thermal studies of 1-methyl-2,6-dimethyl-4-hydroxypyridinium chloride monohydrate and bromide monohydrate. Spectrochim Acta A Mol Biomol Spectrosc (2007) 1.08
Further delineation of the 22q13 deletion syndrome. Clin Dysmorphol (2005) 1.08
Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency. Am J Hum Genet (1992) 1.06
Clinical measures to assess the practice and efficiency of breast self-examination. Cancer (1986) 1.05
Ritodrine in the treatment of preterm labor: second Danish Multicenter Study. Obstet Gynecol (1986) 1.04
Comparative genomic hybridization reveals non-random chromosomal aberrations in early preinvasive cervical lesions. Cancer Genet Cytogenet (2001) 1.04
Screening for Down's syndrome using an iso-risk curve based on maternal age and serum alpha-fetoprotein level. Br J Obstet Gynaecol (1987) 1.03
Health Belief Model variables as predictors of screening mammography utilization. J Behav Med (1994) 1.03
Choroideremia in interstitial deletion of the X chromosome. Ophthalmic Paediatr Genet (1986) 1.02
Late first-trimester invasive prenatal diagnosis: results of an international randomized trial. Obstet Gynecol (2004) 1.01
Enlarged chromosome No. 1 in a patient with primary amenorrhoea. Cytogenetics (1965) 1.00
Assessment of changes in coagulation in parturients with preeclampsia using thromboelastography. Anesthesiology (1999) 0.99
The frequency of chromosome aberrations in tall men with special reference to 47, XYY and 47, XXY. Am J Hum Genet (1976) 0.99
A clinical and cytogenetical study of XX male. Hereditas (1969) 0.98
Simultaneous confocal recording of multiple fluorescent labels with improved channel separation. J Microsc (1994) 0.98
Actin filament organization of the Dunning R3327 rat prostatic adenocarcinoma system: correlation with metastatic potential. Cancer Res (1986) 0.98
Dignity in dying: a preliminary study of patients in the last three days of life. J Palliat Care (1996) 0.97
Selective miscarriage of Down's syndrome fetuses in women aged 35 years and older. Br J Obstet Gynaecol (1995) 0.97
Nephrobronchial fistula - a case report. Int Urol Nephrol (2007) 0.95
Automatic classification of chromosomes as part of a routine system for clinical analysis. Cytometry (1986) 0.95
Relationship between infant birth weight </=2000 g and maternal zinc levels at Muhimbili National Hospital, Dar Es Salaam, Tanzania. J Trop Pediatr (2005) 0.95
LSD in mice: abnormalities in meiotic chromosomes. Science (1968) 0.94
Studies on meiotic chromosomes in infertile men and controls with normak karyotypes. J Reprod Fertil (1973) 0.94
A familial, balanced 2-5 translocation associated with trisomy 21 in one individual. Hum Hered (1974) 0.93
Stimulation of amniotic fluid cells by fibroblast growth factor. Clin Genet (1978) 0.93
Semiautomated chromosome analysis. A clinical test. Clin Genet (1985) 0.93
Primary amenorrhea. A study of 101 cases. Fertil Steril (1966) 0.92
Is screening for ovarian cancer worthwhile? J Med Screen (1994) 0.91
Y-22 translocation in a YY male. Cytogenet Cell Genet (1973) 0.90
Assessing platelet and fibrinogen contribution to clot strength using modified thromboelastography in pregnant women. Anesth Analg (1999) 0.90
Cytoreductive surgery for metastatic testis cancer: tissue analysis of retroperitoneal masses after chemotherapy. J Urol (1982) 0.90
Administration of nitrous oxide in normal subjects. Evaluation of systems of gas delivery for their clinical use and hemodynamic effects. Chest (1977) 0.90
Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization. Prenat Diagn (1992) 0.90
Colour vision deficiency in on of two presumably monozygotic twins with secondary amenorrhoea. Ann Hum Genet (1969) 0.89
Chorionic villus culture for prenatal diagnosis of chromosome defects: reduction of the long-term cultivation time. Prenat Diagn (1989) 0.89
InJection adaptable fine ionization source ('JaFIS') for continuous flow nano-electrospray. Rapid Commun Mass Spectrom (1998) 0.89
A culture vessel for amniotic fluid cells allowing faster preparation of chromosome slides. Prenat Diagn (1985) 0.89
Indication of primary immune deficiency in Fanconi's anemia. Acta Paediatr Scand (1977) 0.88
High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes. Eur J Hum Genet (2000) 0.88
A 5;7, 5;12 double reciprocal translocation in a normal mother and a 5;7 translocation with a recombinant chromosome 5 in her normal child. J Med Genet (1981) 0.88
Optimization of DOP-PCR amplification of DNA for high-resolution comparative genomic hybridization analysis. Cytometry (2001) 0.87
A randomized, controlled trial comparing lidocaine periprostatic nerve block, diclofenac suppository and both for transrectal ultrasound guided biopsy of prostate. J Urol (2005) 0.86
Thromboelastographic changes in healthy parturients and postpartum women. Anesth Analg (1997) 0.85
Biomonitoring of genotoxic exposure among stainless steel welders. Mutat Res (1992) 0.85
Patient reporting and doctor recognition of dyspnoea in a comprehensive cancer centre. Intern Med J (2006) 0.84
Public interest warning: should we ban wooden/ornamental toilet seats for male infants? BJU Int (2008) 0.84
Microspectrophotometry of trypsin-Leishman-stained human chromosomes. Nature (1973) 0.84
Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH. Am J Hum Genet (1996) 0.84
Aneuploidy as a marker for carcinoma-in-situ of the testis. Acta Pathol Microbiol Scand A (1981) 0.84
Diagnostic yield by supplementing prenatal metaphase karyotyping with MLPA for microdeletion syndromes and subtelomere imbalances. Prenat Diagn (2010) 0.84
A test of a climate room for preparation of chromosome slides. Clin Genet (1985) 0.84
Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases. Ann Genet (2004) 0.83
New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report. BMJ (1992) 0.83
Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial. Prenat Diagn (1997) 0.82
Detection of chromosomal aberrations in seminomatous germ cell tumours using comparative genomic hybridization. Genes Chromosomes Cancer (1997) 0.82