Clinical Manifestations of Partial Trisomy 2p von Lurie, Iosif W.

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Partial trisomy 4q and preaxial limb defects von Lurie, Iosif W.

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4q32-q35 and 6q16-q22 are valuable candidate regions for split hand foot malformation von Niedrist, Dunja, Lurie, Iosif W, Schinzel, Albert

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A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations von Bravo-Oro, Antonio, Lurie, Iosif W., Elizondo-Cárdenas, Gabriela, Peña-Zepeda, Claudia, Salazar-Martínez, Abel, Correa-González, Cecilia, Castrillo, José Luis, Avila, Silvia, Esmer, Carmen

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Kidney abnormalities in persons with monosomy 15q26 von Lurie, Iosif W.

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Unbalanced Translocations Involving Chromosome Region 10q25.3q26.3 in Patients with Intellectual Disability and Complex Phenotypes von Hryshchenko, Nataliya V., Bychkova, Ganna M., Tavokina, Lyubov V., Brovko, Anton O., Graziano, Claudio, Soloviov, Oleksandr O., Hettinger, Joe A., Patsalis, Philippos C., Lurie, Iosif W., Livshits, Ludmila A.

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Structural autosomal imbalance and oesophageal defects: Addendum to the article by Felix et al. (2007) von Lurie, Iosif W

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Probability rate of unbalanced offspring at birth and risk of unfavorable pregnancy outcomes in families of carriers of chromosomal reciprocal translocations involving chromosome 7 von Kozłowska, Katarzyna, Panasiuk, Barbara, Stasiewicz-Jarocka, Beata, Lurie, Iosif W, Chrzanowska, Krystyna, Lenkiewicz, Marzena, Gutkowska, Anna, Iliszko, Mariola, Midro, Alina T

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Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation von Kotzot, Dieter, Schmitt, Silke, Bernasconi, Fabiana, Robinson, Wendy P., Lurie, Iosif W., Ilyina, Helena, Méhes, Károly, Hamel, Ben C.J., Otten, Barto J., Hergersberg, Martin, Werder, Edmond, Schoenle, Eugen, Schinzel, Albert

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4q32―q35 and 6q16―q22 are valuable candidate regions for split hand/foot malformation von NIEDRIST, Dunja, LURIE, Iosif W, SCHINZEL, Albert

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Probability rates for different pregnancy outcomes in carriers of reciprocal chromosomal translocations involving chromosome 13 von Panasiuk, Barbara, Dawidowska, Wioletta K, Stasiewicz-Jarocka, Beata, Lurie, Iosif W, Midro, Alina T

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Phenotypic spectrum of tetrasomy 12p and prenatal counseling: potential underestimation of severity von Lurie, Iosif W.

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Distal trisomy 10q and limb defects von Lurie, Iosif W.

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Genetics of the Costello syndrome von Lurie, Iosif W.

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Atrioventricular septal defects: Possible etiologic differences between complete and partial defects von Loffredo, Christopher A., Hirata, Jeffrey, Wilson, P. David, Ferencz, Charlotte, Lurie, Iosif W.

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Isochromosome 18p results from maternal meiosis II nondisjunction von Kotzot, D, Bundscherer, G, Bernasconi, F, Brecevic, L, Lurie, I W, Basaran, S, Baccicchetti, C, Höller, A, Castellan, C, Braun-Quentin, C, Pfeiffer, R A, Schinzel, A

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Trisomy 2p: Analysis of unusual phenotypic findings von Lurie, Iosif W., Ilyina, Helena G., Gurevich, Dora B., Rumyantseva, Natalja V., Naumchik, Irena V., Castellan, Claudio, Hoeller, Adelheid, Schinzel, Albert

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No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation von Kotzot, Dieter, Lurie, Iosif W, Méhes, Károly, Werder, Edmond, Schinzel, Albert

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VACTERL-hydrocephaly, DK-phocomelia, and cerebro-cardio-radio-reno-rectal community von Lurie, Iosif W., Ferencz, Charlotte

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Letter to the editor: Familial omphalocele and recurrence risk von Lurie, Iosif W., Ilyina, Helena G., Opitz, John M.

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