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Prenatal Diagnosis|January 22, 2005
A novel L1CAM mutation with L1 spectrum disordersFatma Silan, Ismail Ozdemir, Willy Lissens
Prenatal Diagnosis|January 22, 2005
DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Brage S Andresen, Ernst Christensen, et al.
Prenatal Diagnosis|January 22, 2005
Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locusE K Bijlsma, A C Knegt, C M Bilardo, et al.
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|February 16, 2005
Prenatal diagnosis of Sanfilippo syndromeJohn J Hopwood
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.
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