Sherman SL - Search Results

1

Paternal nondisjunction in trisomy 21: excess of male patients.

Petersen MB, Antonarakis SE, Hassold TJ, Freeman SB, Sherman SL, Avramopoulos D, Mikkelsen M. Petersen MB, et al. Among authors: sherman sl. Hum Mol Genet. 1993 Oct;2(10):1691-5. doi: 10.1093/hmg/2.10.1691. Hum Mol Genet. 1993. PMID: 8268923

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. Among authors: sherman sl. 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. Hum Genet. 1994 Oct;94(4):411-7. doi: 10.1007/BF00201603. Hum Genet. 1994. PMID: 7927339

4

Recombination and nondisjunction in humans and flies.

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

5

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

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

6

Counting cross-overs: characterizing meiotic recombination in mammals.

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

7

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. Am J Hum Genet. 1995 Oct;57(4):867-74. Am J Hum Genet. 1995. PMID: 7573048 Free PMC article.

8

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination.

Sherman SL, Petersen MB, Freeman SB, Hersey J, Pettay D, Taft L, Frantzen M, Mikkelsen M, Hassold TJ. Sherman SL, et al. Hum Mol Genet. 1994 Sep;3(9):1529-35. doi: 10.1093/hmg/3.9.1529. Hum Mol Genet. 1994. PMID: 7833907

9

Non-disjunction in human sperm: evidence for an effect of increasing paternal age.

Griffin DK, Abruzzo MA, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ. Griffin DK, et al. Among authors: sherman sl. Hum Mol Genet. 1995 Dec;4(12):2227-32. doi: 10.1093/hmg/4.12.2227. Hum Mol Genet. 1995. PMID: 8634691

10

Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.

Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, Hersey J, Gu Y, Shen J, Saker D, May KM, Avramopoulos D, Petersen MB, Hallberg A, Mikkelsen M, Hassold TJ, Sherman SL. Lamb NE, et al. Among authors: sherman sl. Nat Genet. 1996 Dec;14(4):400-5. doi: 10.1038/ng1296-400. Nat Genet. 1996. PMID: 8944019

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

441 results

Search Page

Filters