Berend SA - Search Results

1

Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy.

Berend SA, Feldman GL, McCaskill C, Czarnecki P, Van Dyke DL, Shaffer LG. Berend SA, et al. Am J Med Genet. 1999 Jan 29;82(3):275-81. doi: 10.1002/(sici)1096-8628(19990129)82:3<275::aid-ajmg15>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10215554

2

Familial complex chromosomal rearrangement resulting in a recombinant chromosome.

Berend SA, Bodamer OA, Shapira SK, Shaffer LG, Bacino CA. Berend SA, et al. Am J Med Genet. 2002 May 15;109(4):311-7. doi: 10.1002/ajmg.10334. Am J Med Genet. 2002. PMID: 11992486

3

Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocations.

Berend SA, Bejjani BA, McCaskill C, Shaffer LG. Berend SA, et al. Am J Med Genet. 2002 Sep 1;111(4):362-5. doi: 10.1002/ajmg.10566. Am J Med Genet. 2002. PMID: 12210293

4

Parental origin and timing of de novo Robertsonian translocation formation.

Bandyopadhyay R, Heller A, Knox-DuBois C, McCaskill C, Berend SA, Page SL, Shaffer LG. Bandyopadhyay R, et al. Among authors: berend sa. Am J Hum Genet. 2002 Dec;71(6):1456-62. doi: 10.1086/344662. Epub 2002 Nov 6. Am J Hum Genet. 2002. PMID: 12424707 Free PMC article. Review.

5

Mosaicism in a patient with Down syndrome reveals post-fertilization formation of a Robertsonian translocation and isochromosome.

Bandyopadhyay R, McCaskill C, Knox-Du Bois C, Zhou Y, Berend SA, Bijlsma E, Shaffer LG. Bandyopadhyay R, et al. Among authors: berend sa. Am J Med Genet A. 2003 Jan 15;116A(2):159-63. doi: 10.1002/ajmg.a.10113. Am J Med Genet A. 2003. PMID: 12494435

6

Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.

Berend SA, Page SL, Atkinson W, McCaskill C, Lamb NE, Sherman SL, Shaffer LG. Berend SA, et al. Am J Hum Genet. 2003 Feb;72(2):488-95. doi: 10.1086/367547. Epub 2002 Dec 23. Am J Hum Genet. 2003. PMID: 12506337 Free PMC article.

7

Molecular analysis of mosaicism for two different de novo acrocentric rearrangements demonstrates diversity in Robertsonian translocation formation.

Berend SA, Canún S, McCaskill C, Page SL, Shaffer LG. Berend SA, et al. Am J Med Genet. 1998 Nov 16;80(3):252-9. doi: 10.1002/(sici)1096-8628(19981116)80:3<252::aid-ajmg14>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9843048

8

Pure trisomy 10p involving an isochromosome 10p.

Berend SA, Shaffer LG, Bejjani BA. Berend SA, et al. Clin Genet. 1999 May;55(5):367-71. doi: 10.1034/j.1399-0004.1999.550512.x. Clin Genet. 1999. PMID: 10422809

9

Deletion (9) (p13.1 p21.1).

Scaglia F, Bodamer OA, Berend SA, Adam LR, Shaffer LG. Scaglia F, et al. Among authors: berend sa. Am J Med Genet. 2000 Mar 13;91(2):113-5. Am J Med Genet. 2000. PMID: 10748408

10

Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes.

Berend SA, Horwitz J, McCaskill C, Shaffer LG. Berend SA, et al. Am J Hum Genet. 2000 Jun;66(6):1787-93. doi: 10.1086/302916. Epub 2000 Apr 19. Am J Hum Genet. 2000. PMID: 10775524 Free PMC article.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

20 results

Search Page

Filters