Sherman S - Search Results

1

Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.

Hassold T, Merrill M, Adkins K, Freeman S, Sherman S. Hassold T, et al. Among authors: sherman s. Am J Hum Genet. 1995 Oct;57(4):867-74. Am J Hum Genet. 1995. PMID: 7573048 Free PMC article.

2

Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects.

Allen EG, Freeman SB, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SL. Allen EG, et al. Hum Genet. 2009 Feb;125(1):41-52. doi: 10.1007/s00439-008-0603-8. Epub 2008 Dec 3. Hum Genet. 2009. PMID: 19050929 Free PMC article.

3

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns.

Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. Zaragoza MV, et al. Among authors: sherman s. Hum Genet. 1994 Oct;94(4):411-7. doi: 10.1007/BF00201603. Hum Genet. 1994. PMID: 7927339

4

Trisomy in humans: incidence, origin and etiology.

Hassold T, Hunt PA, Sherman S. Hassold T, et al. Among authors: sherman s. Curr Opin Genet Dev. 1993 Jun;3(3):398-403. doi: 10.1016/0959-437x(93)90111-2. Curr Opin Genet Dev. 1993. PMID: 8353412 Review.

5

The origin of trisomy in humans.

Hassold T, Sherman S, Hunt PA. Hassold T, et al. Among authors: sherman s. Prog Clin Biol Res. 1995;393:1-12. Prog Clin Biol Res. 1995. PMID: 8545442 No abstract available.

6

Recombination and nondisjunction in humans and flies.

Koehler KE, Hawley RS, Sherman S, Hassold T. Koehler KE, et al. Among authors: sherman s. Hum Mol Genet. 1996;5 Spec No:1495-504. doi: 10.1093/hmg/5.supplement_1.1495. Hum Mol Genet. 1996. PMID: 8875256 Review.

7

FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidy.

Hixon M, Millie E, Judis LA, Sherman S, Allran K, Taft L, Hassold T. Hixon M, et al. Among authors: sherman s. Hum Genet. 1998 Dec;103(6):654-7. doi: 10.1007/s004390050886. Hum Genet. 1998. PMID: 9921898

8

Down syndrome: genetic recombination and the origin of the extra chromosome 21.

Hassold T, Sherman S. Hassold T, et al. Among authors: sherman s. Clin Genet. 2000 Feb;57(2):95-100. doi: 10.1034/j.1399-0004.2000.570201.x. Clin Genet. 2000. PMID: 10735628 Review.

9

Counting cross-overs: characterizing meiotic recombination in mammals.

Hassold T, Sherman S, Hunt P. Hassold T, et al. Among authors: sherman s. Hum Mol Genet. 2000 Oct;9(16):2409-19. doi: 10.1093/hmg/9.16.2409. Hum Mol Genet. 2000. PMID: 11005796 Review.

10

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.

Hassold TJ, Sherman SL, Pettay D, Page DC, Jacobs PA. Hassold TJ, et al. Among authors: sherman sl. Am J Hum Genet. 1991 Aug;49(2):253-60. Am J Hum Genet. 1991. PMID: 1867189 Free PMC article.

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