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Prenatal Diagnosis|July 19, 2002
Womens' preference in Down syndrome screeningIrene M de Graaf, Tjeerd Tijmstra, Otto P Bleker, et al.Prenatal Diagnosis|May 1, 1995
Sonographically determined anomalies and outcome in 170 chromosomally abnormal fetusesJ W Wladimiroff, W R Bhaggoe, M Kristelijn, et al.Prenatal Diagnosis|May 1, 1995
New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined populationJ L Halliday, L F Watson, J Lumley, et al.Prenatal Diagnosis|May 1, 1995
A misdiagnosis of X-linked adrenoleukodystrophy in cultured chorionic villus cells by the measurement of very long chain fatty acidsR G Gray, A Green, T Cole, et al.Prenatal Diagnosis|June 1, 1995
The natural history of fetal cytomegalovirus infection as assessed by serial ultrasound and fetal blood sampling: a case reportM L Watt-Morse, S A Laifer, L M HillPrenatal Diagnosis|June 1, 1995
Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart diseaseM L Whiteford, J Coutts, L al-Roomi, et al.Prenatal Diagnosis|December 1, 1993
Co-amplification of the cystic fibrosis delta F508 mutation with the HLA DQA1 sequence in single cell PCR: implications for improved assessment of polar bodies and blastomeres in preimplantation diagnosisR Wu, H Cuppens, I Buyse, et al.Prenatal Diagnosis|December 1, 1993
Asymptomatic carrier of two CFTR mutations: consequences for prenatal diagnosis?C Verlingue, A David, M P Audrezet, et al.Prenatal Diagnosis|February 1, 1994
Maternal serum free beta hCG screening: results of studies including 480 cases of Down syndromeJ N Macri, K Spencer, K Garver, et al.Prenatal Diagnosis|August 1, 1995
A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nucleiD van Opstal, J O van Hemel, B H Eussen, et al.Pageof 695