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Prenatal Diagnosis|January 26, 2002
Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesisChih-Ping Chen, Schu-Rern Chern, Shin-Hua Du, et al.Prenatal Diagnosis|January 26, 2002
Prenatal diagnosis of Joubert syndrome: a case reportHalil Aslan, Volkan Ulker, E Mahir Gulcan, et al.Prenatal Diagnosis|January 26, 2002
Mitochondrial DNA depletion presenting prenatally with skin edema and multisystem disease immediately after birthShmuel Arnon, Rami Aviram, Tzipora Dolfin, et al.Prenatal Diagnosis|January 26, 2002
Detection of fetal cells in intrauterine lavage samples collected in the first trimester of pregnancyRiccardo Cioni, Cecilia Bussani, Benedetta Scarselli, et al.Prenatal Diagnosis|January 26, 2002
A negative second trimester triple test and absence of specific ultrasonographic markers may decrease the need for genetic amniocentesis in advanced maternal age by 60%D J D Rosen, I Kedar, A Amiel, et al.Prenatal Diagnosis|April 5, 2001
Intrauterine rescue transfusion in monochorionic multiple pregnancies with recent single intrauterine deathS Tanawattanacharoen, M J Taylor, E A Letsky, et al.Prenatal Diagnosis|April 5, 2001
An umbilical cord teratoma in a 17-week-old fetusD C Satgé, M A Laumond, F Desfarges, et al.Prenatal Diagnosis|April 5, 2001
Klippel-Trenaunay-Weber (KTW) syndrome: the use of in utero magnetic resonance imaging (MRI) in a prospective diagnosisW L Martin, K M Ismail, V Brace, et al.Prenatal Diagnosis|April 5, 2001
Role of amniotic fluid interphase fluorescence in situ hybridization (FISH) analysis in patient managementW Cheong Leung, D Chitayat, G Seaward, et al.Prenatal Diagnosis|September 12, 2002
Prenatal diagnosis and carrier detection for Athabascan severe combined immunodeficiency diseaseLanying Li, Yungui Zhou, Junhua Wang, et al.Pageof 699