Inter- and Intrachromosomal Rearrangements Are Both Involved in the Origin of 15q11-q13 Deletions in Prader-Willi Syndrome von Carrozzo, Romeo, Rossi, Elena, Christian, Susan L., Kittikamron, Kirk, Livieri, Chiara, Corrias, Andrea, Pucci, Lucia, Fois, Alberto, Bosio, Laura, Simi, Paolo, Beccaria, Luciano, Zuffardi, Orsetta, Ledbetter, David H.

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Two 22q telomere deletions serendipitously detected by FISH von Precht, K S, Lese, C M, Spiro, R P, Huttenlocher, P R, Johnston, K M, Baker, J C, Christian, S L, Kittikamron, K, Ledbetter, D H

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Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus von Christian, Susan L., Rich, Barry H., Loebl, Charli, Israel, Jeannette, Vasa, Rohitkumar, Kittikamron, Kirk, Spiro, Rhonda, Rosenfield, Robert, Ledbetter, David H.

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Preparative-Scale Purification of RNA Using an Efficient Method Which Combines Gel Electrophoresis and Column Chromatography von Cunningham, Lynette, Kittikamron, Kirk, Lu, Yi

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Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation von Matsumoto, N, Pilz, D T, Fantes, J A, Kittikamron, K, Ledbetter, D H

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Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal mellitus von CHRISTIAN, S. L, RICH, B. H, LOEBL, C, ISRAEL, J, VASA, R, KITTIKAMRON, K, SPIRO, R, ROSENFIELD, R, LEDBETTER, D. H

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