A tribute to Malcolm Ferguson-Smith, founding editor of Prenatal DiagnosisBIANCHI, Diana W; RODECK, Charles H.Prenatal diagnosis. 2007, Vol 27, Num 9, pp 854-855, issn 0197-3851, 2 p.Article

Prenatal diagnosis of septal agenesis with normal pituitary functionCELENTANO, Claudio; PREFUMO, Federico; LIBERATI, Marco et al.Prenatal diagnosis. 2006, Vol 26, Num 11, pp 1075-1077, issn 0197-3851, 3 p.Article

Prenatal diagnosis of Juberg-Hayward syndromeCOUVREUR-LIONNAIS, Stéphanie; ROUSSEAU, Thierry; LAURENT, Nicole et al.Prenatal diagnosis. 2005, Vol 25, Num 2, pp 172-175, issn 0197-3851, 4 p.Article

Interstitial deletion del(10)(q25.2q25.3 ∼ 26.11) : case report and review of the literatureKEHRER-SAWATZKI, Hildegard; DAUMILLER, Eva; MÜLLER-NAVIA, Jutta et al.Prenatal diagnosis. 2005, Vol 25, Num 10, pp 954-959, issn 0197-3851, 6 p.Article

What prenatal diagnosis should be offered in multiple pregnancy?BHIDE, Amaranth; THILAGANATHAN, Baskaran.Baillière's best practice & research. Clinical obstetrics & gynaecology. 2004, Vol 18, Num 4, pp 531-542, issn 1521-6934, 12 p.Article

Scanning for chorionicity : comparison between sonographers and perinatologistsWEISZ, Boaz; PANDYA, Pranav; DAVE, Raj et al.Prenatal diagnosis. 2005, Vol 25, Num 9, pp 835-838, issn 0197-3851, 4 p.Article

Hemimegalencephaly: Prenatal Diagnosis and OutcomeALVAREZ, Maria; GARCIA-DIAZ, Lutgardo; MARQUEZ, Javier et al.Fetal diagnosis and therapy. 2011, Vol 30, Num 3, pp 234-238, issn 1015-3837, 5 p.Article

Prenatal diagnosis of sickle syndromes in India : dilemmas in counsellingCOLAH, Roshan; SURVE, Reema; NADKARNI, Anita et al.Prenatal diagnosis. 2005, Vol 25, Num 5, pp 345-349, issn 0197-3851, 5 p.Article

Coping with termination of pregnancy for fetal abnormality in a supportive environmentGEERINCK-VERCAMMEN, C. R; KANHAI, H. H. H.Prenatal diagnosis. 2003, Vol 23, Num 7, pp 543-548, issn 0197-3851, 6 p.Article

Spondylothoracic dysplasia : Prenatal diagnosis and the problems of nosologic overlapPHADKE, Shubha R; PATIL, Siddramappa J; KUMARI, Niraj et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 8, pp 899-902, issn 1552-4825, 4 p.Article

Prenatal diagnosis of triple X using fetal cells obtained by endocervical lavageXIAO XI ZHAO; SUZUMORI, Kaoru; SATO, Takeshi et al.Prenatal diagnosis. 2003, Vol 23, Num 7, pp 549-551, issn 0197-3851, 3 p.Article

Fundamental problems and solutions concerning genetic testing (2^nd part)BENNET, Tierney.Alpha omega (Roma). 2002, Vol 5, Num 3, pp 473-497, issn 1126-8557, 25 p.Article

Residual risk for cytogenetic abnormalities after prenatal diagnosis by interphase fluorescence in situ hybridization (FISH)HOMER, Jeanne; BHATT, Sucheta; BING HUANG et al.Prenatal diagnosis. 2003, Vol 23, Num 7, pp 566-571, issn 0197-3851, 6 p.Article

Male or female, we will create them: The ethics of sex selection for non-medical reasonsHEYD, David.Ethical perspectives - Katholieke Universiteit Leuven. 2003, Vol 10, Num 2, pp 204-214, issn 1370-0049, 11 p.Article

Amniocentesis Performed for Karyotyping after Identified Ultrasonographic Abnormalities: What to Expect?GAUDRY, Patrice; ESVAN, Maxime; MEYNARD, Jean-Baptiste et al.Fetal diagnosis and therapy. 2012, Vol 31, Num 1, pp 55-62, issn 1015-3837, 8 p.Article

Effect of cord puncture site in cordocentesis at mid-pregnancy on pregnancy outcomesTANGSHEWINSIRIKUL, Chayada; WANAPIRAK, Chanane; PIYAMONGKOL, Wirawit et al.Prenatal diagnosis. 2011, Vol 31, Num 9, pp 861-864, issn 0197-3851, 4 p.Article

Prenatal diagnosis of lobar bronchial atresiaBONNEFOY, C; BLANC, P; GALLOT, D et al.Ultrasound in obstetrics & gynecology. 2011, Vol 37, Num 1, pp 110-112, issn 0960-7692, 3 p.Article

Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non-selective application of a MLPA-based extended prenatal panel in routine prenatal diagnosisKONIALIS, Christopher; HAGNEFELT, Birgitta; SEVASTIDOU, Sophia et al.Prenatal diagnosis. 2011, Vol 31, Num 6, pp 571-577, issn 0197-3851, 7 p.Article

Current and emerging techniques of fetal cell separation from maternal bloodKAVANAGH, D. M; KERSAUDY-KERHOAS, M; DHARIWAL, R. S et al.Journal of chromatography. B. 2010, Vol 878, Num 22, pp 1905-1911, issn 1570-0232, 7 p.Article

High-resolution array genomic hybridization in prenatal diagnosisFRIEDMAN, J. M.Prenatal diagnosis. 2009, Vol 29, Num 1, pp 20-28, issn 0197-3851, 9 p.Conference Paper

Isolated or non-isolated duodenal obstruction : perinatal outcome following prenatal or postnatal diagnosisCOHEN-OVERBEEK, T. E; GRIJSEELS, E. W. M; NIEMEIJER, N. D et al.Ultrasound in obstetrics & gynecology. 2008, Vol 32, Num 6, pp 784-792, issn 0960-7692, 9 p.Article

Trisomy 18: Fetal ultrasound findings at different gestational agesVIORA, E; ZAMBONI, C; MORTARA, G et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 6, pp 553-557, issn 1552-4825, 5 p.Article

Le fantasme de l'enfant parfait et les fantômes de l'eugénisme = The phantasm of the perfect child and phantoms of eugenismPICONE, O; FRYDMAN, R.Revue médicale de Bruxelles. 2007, Vol 28, Num 3, pp 150-152, issn 0035-3639, 3 p.Article

Termination of pregnancy for fetal anomalyASLAN, H; YILDIRIM, G; ONGUT, C et al.International journal of gynaecology and obstetrics. 2007, Vol 99, Num 3, pp 221-224, issn 0020-7292, 4 p.Article

Whole genome amplification from single cells in preimplantation genetic diagnosis and prenatal diagnosisWEN PENG; TAKABAYASHI, Haruo; IKAWA, Kazumi et al.European journal of obstetrics, gynecology, and reproductive biology. 2007, Vol 131, Num 1, pp 13-20, issn 0301-2115, 8 p.Article