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

Volltext

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

Volltext

Maternal uniparental disomy 7 : review and further delineation of the phenotype von KOTZOT, D, BALMER, D, TARIVERDIAN, G, SCHINZEL, A, BAUMER, A, CHRZANOWSKA, K, HAMEL, B. C. J, ILYINA, H, KRAJEWSKA-WALASEK, M, LURIE, I. W, OTTEN, B. J, SCHOENLE, E

Volltext

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation von Kotzot, D, Lurie, IW, Méhes, K, Werder, E, Schinzel, A

Volltext

Pallister-Hall and McKusick-Kaufmann syndromes von Lurie, I W

Volltext

"Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocation von Mikelsaar, R V, Lurie, I W, Ilus, T E

Volltext

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

Volltext

Association of amelia and anal atresia is separate from VACTERL association von Lurie, I W

Volltext

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

Volltext

Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus von KOTZOT, D, BERNASCONI, F, BRECEVIC, L, ROBINSON, W. P, KISS, P, KOSZTOLANYI, G, LURIE, I. W, SUPERTI-FURGA, A, SCHINZEL, A

Volltext

Trisomy 4p and ocular defects von Lurie, I W, Samochvalov, V A

Volltext

Atypical case of Aarskog syndrome von Mikelsaar, R V, Lurie, I W

Volltext

Heart disease in infancy: A window to the world of fetal cardiology von Lurie, Iosif W., Ferencz, Charlotte, Brenner, Joel I.

Volltext

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

Volltext

'Microgastria--limb reduction' complex with congenital heart disease and twinning von Lurie, I W, Magee, C A, Sun, C C, Ferencz, C

Volltext

Distal trisomy 14q von Mikelsaar, R V, Ilus, T A, Lurie, I W

Volltext

Genetics of the Costello syndrome von Lurie, Iosif W.

Volltext

Down's syndrome with 45 chromosomes von Lurie, I W

Volltext

Further study of genetic interactions: Loss of short arm material in patients with ring chromosome 4 changes developmental pattern of del(4)(q33) von Lurie, Iosif W.

Volltext

Interrupted aortic arch: An epidemiologic study von Loffredo, Christopher A., Ferencz, Charlotte, Wilson, P. David, Lurie, Iosif W.

Volltext