Freeman 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: freeman 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

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. Among authors: freeman s. Hum Mol Genet. 1997 Sep;6(9):1391-9. doi: 10.1093/hmg/6.9.1391. Hum Mol Genet. 1997. PMID: 9285774

4

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.

5

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

6

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

7

Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.

Yoon PW, Freeman SB, Sherman SL, Taft LF, Gu Y, Pettay D, Flanders WD, Khoury MJ, Hassold TJ. Yoon PW, et al. Among authors: freeman sb. Am J Hum Genet. 1996 Mar;58(3):628-33. Am J Hum Genet. 1996. PMID: 8644722 Free PMC article.

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

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. Among authors: freeman v, freeman s. Am J Med Genet Suppl. 1990;7:175-81. doi: 10.1002/ajmg.1320370735. Am J Med Genet Suppl. 1990. PMID: 1981476

10

Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemia.

Lorber BJ, Freeman SB, Hassold T, Ragab AH, Vega RA, Cockwell AE, Jacobs PA, Radford M, Doyle J, Dubé ID, et al. Lorber BJ, et al. Among authors: freeman sb. Genes Chromosomes Cancer. 1992 Apr;4(3):222-7. doi: 10.1002/gcc.2870040306. Genes Chromosomes Cancer. 1992. PMID: 1382563

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