Prenatal Diagnosis of a Fetus with Terminal Deletion of Chromosome 1 (q43) in First-Trimester Screening: Is There a Characteristic Antenatal 1q Deletion Phenotype? A Case Report and Review of the Literature

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Fetal Diagnosis and Therapy, Vol. 29, Iss. 3, 2010-12 ,pp. : 253-256

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Prenatal Diagnosis of a Partial Monosomy 7q11→q31 in a Fetus with Split Foot

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Fetal Diagnosis and Therapy, Vol. 20, Iss. 2, 2005-02 ,pp. : 132-135

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Prenatal Diagnosis of a Fetus Affected with Down Syndrome and Deletion 1p36 Syndrome by Fluorescence in situ Hybridization and Spectral Karyotyping

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Fetal Diagnosis and Therapy, Vol. 19, Iss. 4, 2004-06 ,pp. : 356-360

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Prenatal Detection of an Interstitial Deletion in 4p15 in a Fetus with an Increased Nuchal Skin Fold Measurement

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Fetal Diagnosis and Therapy, Vol. 20, Iss. 1, 2004-12 ,pp. : 58-63

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Prenatal Diagnosis of a Fetus with Unbalanced Translocation (4;13)(p16;q32) with Overlapping Features of Patau and Wolf-Hirschhorn Syndromes

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Fetal Diagnosis and Therapy, Vol. 17, Iss. 6, 2002-10 ,pp. : 347-351

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