9237260 1424245 1456285 1332362 8456836 12384779 8388170 1951447 7977469 1746608 1347469 9109809 8129028 16629925 9399882 1746607 2090424 1679180 1362225 7625442 1856831 1427794 1938783 8733057 30020076 2073833 1672177 1684091 1611213 8389098 1919571 - Search Results

Year	Number of Results
1990	3
1991	15
1992	19
1993	15
1994	6
1995	5
1996	5
1997	7
1998	4
2000	1
2001	2
2002	1
2006	3
2009	1
2010	1
2011	1
2012	2
2014	1
2015	1
2017	1
2018	3
2019	1
2020	2
2021	2
2022	1

1

Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.

Glenn CC, Driscoll DJ, Yang TP, Nicholls RD. Glenn CC, et al. Mol Hum Reprod. 1997 Apr;3(4):321-32. doi: 10.1093/molehr/3.4.321. Mol Hum Reprod. 1997. PMID: 9237260 Review.

2

Clinical, cytogenetic and molecular investigations in three patients with Wolf-Hirschhorn syndrome.

Thies U, Back E, Wolff G, Schroeder-Kurth T, Hager HD, Schröder K. Thies U, et al. Clin Genet. 1992 Oct;42(4):201-5. doi: 10.1111/j.1399-0004.1992.tb03238.x. Clin Genet. 1992. PMID: 1424245

3

Constitutional translocation t(4;22) (q12;q12.2) associated with neurofibromatosis type 2.

Arai E, Ikeuchi T, Karasawa S, Tamura A, Yamamoto K, Kida M, Ichimura K, Yuasa Y, Tonomura A. Arai E, et al. Am J Med Genet. 1992 Sep 15;44(2):163-7. doi: 10.1002/ajmg.1320440209. Am J Med Genet. 1992. PMID: 1456285

4

In search for genes predisposing to epilepsy: motives and methods.

Lindhout D, Sander T, Halley DJ, Kasteleijn-Nolst Trenité DG. Lindhout D, et al. Acta Neurol Scand Suppl. 1992;140:51-8. doi: 10.1111/j.1600-0404.1992.tb04471.x. Acta Neurol Scand Suppl. 1992. PMID: 1332362 Review. No abstract available.

5

Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome.

Freeman SB, May KM, Pettay D, Fernhoff PM, Hassold TJ. Freeman SB, et al. Am J Med Genet. 1993 Mar 1;45(5):625-30. doi: 10.1002/ajmg.1320450522. Am J Med Genet. 1993. PMID: 8456836

6

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE. Monk D, et al. Hum Genet. 2002 Oct;111(4-5):376-87. doi: 10.1007/s00439-002-0777-4. Epub 2002 Aug 16. Hum Genet. 2002. PMID: 12384779

7

Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview.

Knoll JH, Wagstaff J, Lalande M. Knoll JH, et al. Am J Med Genet. 1993 Apr 1;46(1):2-6. doi: 10.1002/ajmg.1320460103. Am J Med Genet. 1993. PMID: 8388170 Review.

8

DNA analysis in patients with lissencephaly type I and other cortical dysplasias.

Oostra BA, de Rijk-van Andel JF, Eussen HJ, van Hemel JO, Halley DJ, Niermeijer MF. Oostra BA, et al. Am J Med Genet. 1991 Sep 1;40(3):383-6. doi: 10.1002/ajmg.1320400328. Am J Med Genet. 1991. PMID: 1951447

9

Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.

Delach JA, Rosengren SS, Kaplan L, Greenstein RM, Cassidy SB, Benn PA. Delach JA, et al. Am J Med Genet. 1994 Aug 1;52(1):85-91. doi: 10.1002/ajmg.1320520117. Am J Med Genet. 1994. PMID: 7977469

10

Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2.

Aughton DJ, Cassidy SB, Whiteman DA, Delach JA, Guttmacher AE. Aughton DJ, et al. Am J Med Genet. 1991 Sep 15;40(4):440-3. doi: 10.1002/ajmg.1320400412. Am J Med Genet. 1991. PMID: 1746608

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

Search Page

Search Results