Driscoll DJ - Search Results

1

Williams CA, Zori RT, Hendrickson J, Stalker H, Marum T, Whidden E, Driscoll DJ. Williams CA, et al. Among authors: driscoll dj. Curr Probl Pediatr. 1995 Aug;25(7):216-31. doi: 10.1016/s0045-9380(06)80036-8. Curr Probl Pediatr. 1995. PMID: 8521718 Review. No abstract available.

2

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.

Driscoll DJ, Waters MF, Williams CA, Zori RT, Glenn CC, Avidano KM, Nicholls RD. Driscoll DJ, et al. Genomics. 1992 Aug;13(4):917-24. doi: 10.1016/0888-7543(92)90001-9. Genomics. 1992. PMID: 1505981

3

Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation.

Williams CA, Angelman H, Clayton-Smith J, Driscoll DJ, Hendrickson JE, Knoll JH, Magenis RE, Schinzel A, Wagstaff J, Whidden EM, et al. Williams CA, et al. Among authors: driscoll dj. Am J Med Genet. 1995 Mar 27;56(2):237-8. doi: 10.1002/ajmg.1320560224. Am J Med Genet. 1995. PMID: 7625452 No abstract available.

4

Cytogenetic and molecular analysis in Angelman syndrome.

Zackowski JL, Nicholls RD, Gray BA, Bent-Williams A, Gottlieb W, Harris PJ, Waters MF, Driscoll DJ, Zori RT, Williams CA. Zackowski JL, et al. Among authors: driscoll dj. Am J Med Genet. 1993 Apr 1;46(1):7-11. doi: 10.1002/ajmg.1320460104. Am J Med Genet. 1993. PMID: 8098583

5

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

Glenn CC, Nicholls RD, Robinson WP, Saitoh S, Niikawa N, Schinzel A, Horsthemke B, Driscoll DJ. Glenn CC, et al. Among authors: driscoll dj. Hum Mol Genet. 1993 Sep;2(9):1377-82. doi: 10.1093/hmg/2.9.1377. Hum Mol Genet. 1993. PMID: 8242060 Free article.

6

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion.

Zori RT, Lupski JR, Heju Z, Greenberg F, Killian JM, Gray BA, Driscoll DJ, Patel PI, Zackowski JL. Zori RT, et al. Among authors: driscoll dj. Am J Med Genet. 1993 Sep 15;47(4):504-11. doi: 10.1002/ajmg.1320470414. Am J Med Genet. 1993. PMID: 8256814

7

Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: prenatal and postnatal late replication studies.

Zori RT, Gray BA, Bent-Williams A, Driscoll DJ, Williams CA, Zackowski JL. Zori RT, et al. Among authors: driscoll dj. Am J Med Genet. 1993 Jun 1;46(4):379-83. doi: 10.1002/ajmg.1320460407. Am J Med Genet. 1993. PMID: 8357008

8

Lack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesis.

Migeon BR, Jeppesen P, Torchia BS, Fu S, Dunn MA, Axelman J, Schmeckpeper BJ, Fantes J, Zori RT, Driscoll DJ. Migeon BR, et al. Among authors: driscoll dj. Am J Hum Genet. 1996 Jan;58(1):161-70. Am J Hum Genet. 1996. PMID: 8554052 Free PMC article.

9

Familial cryptic translocation resulting in Angelman syndrome:implications for imprinting or location of the Angelman gene?

Burke LW, Wiley JE, Glenn CC, Driscoll DJ, Loud KM, Smith AJ, Kushnick T. Burke LW, et al. Among authors: driscoll dj. Am J Hum Genet. 1996 Apr;58(4):777-84. Am J Hum Genet. 1996. PMID: 8644742 Free PMC article.

10

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.

Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD. Saitoh S, et al. Among authors: driscoll dj. Am J Med Genet. 1997 Jan 20;68(2):195-206. Am J Med Genet. 1997. PMID: 9028458

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