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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.Prenatal Diagnosis|August 1, 1993
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndromeG Martini, G Carillo, F Catizone, et al.Prenatal Diagnosis|September 1, 1994
The association between alpha-fetoprotein and beta hCG levels prior to and following chorionic villus sampling in cases that spontaneously miscarriedG Barkai, B Reichman, L Ries, et al.Prenatal Diagnosis|November 1, 1994
MSAFP levels and oesophageal atresiaB N Chodirker, A E Chudley, K M MacDonald, et al.Prenatal Diagnosis|July 1, 1994
Maternal serum markers in second-trimester oligohydramniosF J Los, A M Hagenaars, T E Cohen-Overbeek, et al.Pageof 695