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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.
Prenatal Diagnosis|August 1, 1995
Molecular prenatal diagnosis of 3-hydroxy-3-methylglutaryl CoA lyase deficiencyG A Mitchell, C Jakobs, K M Gibson, et al.
Prenatal Diagnosis|August 1, 1995
Urinary multiple marker screening for Down's syndromeH S Cuckle, R K Iles, I K Sehmi, et al.
Prenatal Diagnosis|August 1, 1995
Prenatal diagnosis of metatropic dwarfismS Manouvrier-Hanu, L Devisme, M C Zelasko, et al.
Prenatal Diagnosis|August 1, 1995
Apparent segregation of null alleles ascribed to deletions of the ornithine transcarbamylase gene in congenital hyperammonaemiaB Segues, J M Rozet, B Gilbert, et al.
Prenatal Diagnosis|August 1, 1993
Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridizationG H Schuring-Blom, M Keijzer, M E Jakobs, et al.
Prenatal Diagnosis|August 1, 1993
Cytogenetic analysis of 2928 CVS samples and 1075 amniocenteses from randomized studiesS Smidt-Jensen, A M Lind, M Permin, et al.
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