Freeman SB - 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: freeman sb. 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: freeman sb. 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

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.

4

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.

Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, Hassold T, Sherman SL. Lamb NE, et al. Hum Mol Genet. 1997 Sep;6(9):1391-9. doi: 10.1093/hmg/6.9.1391. Hum Mol Genet. 1997. PMID: 9285774

5

Trisomy 21: association between reduced recombination and nondisjunction.

Sherman SL, Takaesu N, Freeman SB, Grantham M, Phillips C, Blackston RD, Jacobs PA, Cockwell AE, Freeman V, Uchida I, et al. Sherman SL, et al. Among authors: freeman v, freeman sb. Am J Hum Genet. 1991 Sep;49(3):608-20. Am J Hum Genet. 1991. PMID: 1831960 Free PMC article.

6

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. Among authors: freeman sb. Hum Mol Genet. 1994 Sep;3(9):1529-35. doi: 10.1093/hmg/3.9.1529. Hum Mol Genet. 1994. PMID: 7833907

7

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: freeman sb. Nat Genet. 1996 Dec;14(4):400-5. doi: 10.1038/ng1296-400. Nat Genet. 1996. PMID: 8944019

8

Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans.

Savage AR, Petersen MB, Pettay D, Taft L, Allran K, Freeman SB, Karadima G, Avramopoulos D, Torfs C, Mikkelsen M, Hassold TJ, Sherman SL. Savage AR, et al. Among authors: freeman sb. Hum Mol Genet. 1998 Aug;7(8):1221-7. doi: 10.1093/hmg/7.8.1221. Hum Mol Genet. 1998. PMID: 9668162

9

Risk factors for nondisjunction of trisomy 21.

Sherman SL, Freeman SB, Allen EG, Lamb NE. Sherman SL, et al. Among authors: freeman sb. Cytogenet Genome Res. 2005;111(3-4):273-80. doi: 10.1159/000086900. Cytogenet Genome Res. 2005. PMID: 16192705 Review.

10

Nondisjunction of chromosome 21.

Takaesu N, Jacobs PA, Cockwell A, Blackston RD, Freeman S, Nuccio J, Kurnit DM, Uchida I, Freeman V, Hassold T. Takaesu N, et al. Am J Med Genet Suppl. 1990;7:175-81. doi: 10.1002/ajmg.1320370735. Am J Med Genet Suppl. 1990. PMID: 1981476

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