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Prenatal Diagnosis|February 16, 2005
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter)Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, et al.Prenatal Diagnosis|February 16, 2005
Prenatal diagnosis of Juberg-Hayward syndromeStéphanie Couvreur-Lionnais, Thierry Rousseau, Nicole Laurent, et al.Prenatal Diagnosis|February 16, 2005
Mosaic trisomy (8)(p22 --> pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequencesJ M de Pater, H Y Kroes, M Verschuren, et al.Prenatal Diagnosis|October 1, 1992
Fumarylacetoacetase activity in cultured and non-cultured chorionic villus cells, and assay in two high-risk pregnanciesM J McCormack, E Walker, R G Gray, et al.Prenatal Diagnosis|October 1, 1992
Prenatal analyses in a pregnancy at risk for beta-mannosidosisW J Kleijer, G C Geilen, O P Van Diggelen, et al.Prenatal Diagnosis|November 25, 2003
Trends in elective terminations of pregnancy between 1989 and 2000 in a French county (the Isère)P Guillem, B Fabre, C Cans, et al.Prenatal Diagnosis|November 25, 2003
Prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency in chorionic villi: a novel approachBernadette Chadefaux Vekemans, Jean-Paul Bonnefont, Joëlle Aupetit, et al.Prenatal Diagnosis|November 25, 2003
Meconium peritonitis and pseudo-cyst formation: prenatal diagnosis and post-natal courseF Eckoldt, K S Heling, R Woderich, et al.Prenatal Diagnosis|November 25, 2003
Fetal serum alpha-fetoprotein in alloimmunised pregnanciesJose L Bartha, Gayle Harrison, Phillipa M Kyle, et al.Pageof 695