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Prenatal Diagnosis|August 12, 2004
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafnessDomenico A Coviello, Bruno Brambati, Lucia Tului, et al.Prenatal Diagnosis|August 12, 2004
A case of ring chromosome 22 with deletion of the 22q13.3 region associated with agenesis of the corpus callosum, fornix and septum pellucidumJosé Delcán, María Orera, Rafael Linares, et al.Prenatal Diagnosis|August 12, 2004
Prenatal diagnosis of Pfeiffer syndrome type IIBettina Blaumeiser, Philip Loquet, Wim Wuyts, et al.Prenatal Diagnosis|August 12, 2004
Investigation of lysosomal storage diseases in nonimmune hydrops fetalisMaira G Burin, Ana P Scholz, Rejane Gus, et al.Prenatal Diagnosis|July 2, 2004
QF-PCR-based prenatal detection of aneuploidy in a southeast Asian populationR Quaife, L F Wong, S Y Tan, et al.Prenatal Diagnosis|April 2, 2004
Del(18p) syndrome with increased nuchal translucency in prenatal diagnosisYoung-Mi Kim, Eun-Hee Cho, Jin-Mi Kim, et al.Prenatal Diagnosis|April 2, 2004
The three-vessel and tracheal view of the fetal heart: an in utero sonographic evaluationYaron Zalel, Yifat Wiener, Ronni Gamzu, et al.Prenatal Diagnosis|April 2, 2004
Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria--estimation of applicability of 6 STR markers on chromosomes 21 and 18Silvia Andonova, Radoslava Vazharova, Violeta Dimitrova, et al.Prenatal Diagnosis|April 6, 2004
Effects of triploidy on early human developmentT Philipp, K Grillenberger, E R Separovic, et al.Prenatal Diagnosis|April 6, 2004
The prenatal presentation of congenital erythropoietic porphyria: report of two siblings with elevated maternal serum alpha-fetoproteinNoam Lazebnik, Roee S LazebnikPageof 699