Driscoll DJ - Search Results

1

Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Cassidy SB, et al. Among authors: driscoll dj. Genet Med. 2012 Jan;14(1):10-26. doi: 10.1038/gim.0b013e31822bead0. Epub 2011 Sep 26. Genet Med. 2012. PMID: 22237428 Free article. Review.

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

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.

4

Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.

Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Malcolm S, Pembrey ME, Nicholls RD. Clayton-Smith J, et al. Among authors: driscoll dj. Am J Med Genet. 1993 Oct 1;47(5):683-6. doi: 10.1002/ajmg.1320470519. Am J Med Genet. 1993. PMID: 8266996

5

DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region.

Mowery-Rushton PA, Driscoll DJ, Nicholls RD, Locker J, Surti U. Mowery-Rushton PA, et al. Among authors: driscoll dj. Am J Med Genet. 1996 Jan 11;61(2):140-6. doi: 10.1002/(SICI)1096-8628(19960111)61:2<140::AID-AJMG7>3.0.CO;2-0. Am J Med Genet. 1996. PMID: 8669440

6

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

7

Unexpected familial recurrence in Angelman syndrome.

Connerton-Moyer KJ, Nicholls RD, Schwartz S, Driscoll DJ, Hendrickson JE, Williams CA, Pauli RM. Connerton-Moyer KJ, et al. Among authors: driscoll dj. Am J Med Genet. 1997 Jun 13;70(3):253-60. doi: 10.1002/(sici)1096-8628(19970613)70:3<253::aid-ajmg8>3.0.co;2-x. Am J Med Genet. 1997. PMID: 9188662

8

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.

Ohta T, Buiting K, Kokkonen H, McCandless S, Heeger S, Leisti H, Driscoll DJ, Cassidy SB, Horsthemke B, Nicholls RD. Ohta T, et al. Among authors: driscoll dj. Am J Hum Genet. 1999 Feb;64(2):385-96. doi: 10.1086/302232. Am J Hum Genet. 1999. PMID: 9973277 Free PMC article.

9

Imprinting-mutation mechanisms in Prader-Willi syndrome.

Ohta T, Gray TA, Rogan PK, Buiting K, Gabriel JM, Saitoh S, Muralidhar B, Bilienska B, Krajewska-Walasek M, Driscoll DJ, Horsthemke B, Butler MG, Nicholls RD. Ohta T, et al. Among authors: driscoll dj. Am J Hum Genet. 1999 Feb;64(2):397-413. doi: 10.1086/302233. Am J Hum Genet. 1999. PMID: 9973278 Free PMC article.

10

A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region.

Jong MT, Gray TA, Ji Y, Glenn CC, Saitoh S, Driscoll DJ, Nicholls RD. Jong MT, et al. Among authors: driscoll dj. Hum Mol Genet. 1999 May;8(5):783-93. doi: 10.1093/hmg/8.5.783. Hum Mol Genet. 1999. PMID: 10196367

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

369 results

Search Page