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Prenatal Diagnosis|October 19, 2005
Gorlin syndrome presenting as prenatal chylothorax in a girlD Geneviève, E Walter, P Gorry, et al.Prenatal Diagnosis|October 19, 2005
Prenatal diagnosis of monosomy 4p14-->pter and trisomy 11q25-->qter: clinical presentations and outcomesHsiu-Huei Peng, Tzu-Hao Wang, An-Shine Chao, et al.Prenatal Diagnosis|October 19, 2005
Is there an increased rate of anencephaly in twins?Ido Ben-Ami, Zvika Vaknin, Orit Reish, et al.Prenatal Diagnosis|October 19, 2005
Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotypeUrvashi Surti, Lyndon M Hill, Jeanette Dunn, et al.Prenatal Diagnosis|October 19, 2005
Prenatal detection of deletion 6q13q15 in a complex karyotypeMin Yu, Angela C Obringer, Melissa H Fowler, et al.Prenatal Diagnosis|October 19, 2005
First prenatal molecular diagnosis in a family with holocarboxylase synthetase deficiencySabrina Malvagia, Amelia Morrone, Elisabetta Pasquini, et al.Prenatal Diagnosis|October 19, 2005
Integrated serum screening for Down syndrome in primary obstetric practiceGeorge J Knight, Glenn E Palomaki, Louis M Neveux, et al.Prenatal Diagnosis|October 22, 2005
Population screening for fetal trisomy 21: easy access to screening should be balanced against a uniform ultrasound protocolWilfried J A Gyselaers, Annie J Vereecken, Erik J H Van Herck, et al.Prenatal Diagnosis|November 14, 2009
First trimester maternal serum pregnancy-specific beta-1-glycoprotein (SP1) as a marker of adverse pregnancy outcomeKasper Pihl, Torben Larsen, Inga Laursen, et al.Prenatal Diagnosis|November 1, 1993
Fetal akinesia/hypokinesia sequence: prenatal diagnosis and intra-familial variabilityC A Bacino, L D Platt, A Garber, et al.Pageof 699