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Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

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

In: Human Molecular Genetics, 1995, vol. 4, no. 4, p. 583-587

Consortium of Swiss Academic Libraries

Modification of 15q11 — q13 DNA methylation imprints in unique Angelman and Prader — Willi patients

Glenn, Christopher C. ; Nicholls, Robert D. ; Robinson, Wendy P. ; Saitoh, Shinjl ; Nllkawa, Norlo ; Schlnzel, Albert ; Horsthemke, Bernhard ; Driscoll, Daniel J.

In: Human Molecular Genetics, 1993, vol. 2, no. 9, p. 1377-1382

Consortium of Swiss Academic Libraries

Sex-specific meiotic recombination in the Prader—Willi/Angelman syndrome imprinted region

Robinson, Wendy P. ; Lalande, Marc

In: Human Molecular Genetics, 1995, vol. 4, no. 5, p. 801-806

Consortium of Swiss Academic Libraries

Detection of aberrant DNA methylation in unique Prader — Willi syndrome patients and its diagnostic implications

Buiting, Karin ; Dittrich, Bärbel ; Robinson, Wendy P. ; Guitart, Mirlam ; Abeliovich, Dvorah ; Lerer, Israela ; Horsthemke, Bernhard

In: Human Molecular Genetics, 1994, vol. 3, no. 6, p. 893-895

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