Freeman SB - Search Results

1

Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome.

Freeman SB, May KM, Pettay D, Fernhoff PM, Hassold TJ. Freeman SB, et al. Am J Med Genet. 1993 Mar 1;45(5):625-30. doi: 10.1002/ajmg.1320450522. Am J Med Genet. 1993. PMID: 8456836

2

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

3

Molecular studies of non-disjunction in trisomy 16.

Hassold TJ, Pettay D, Freeman SB, Grantham M, Takaesu N. Hassold TJ, et al. Among authors: freeman sb. J Med Genet. 1991 Mar;28(3):159-62. doi: 10.1136/jmg.28.3.159. J Med Genet. 1991. PMID: 2051452 Free PMC article.

4

Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)].

Freeman SB, Muralidharan K, Pettay D, Blackston RD, May KM. Freeman SB, et al. Am J Med Genet. 1996 Feb 2;61(4):340-4. doi: 10.1002/(SICI)1096-8628(19960202)61:4<340::AID-AJMG7>3.0.CO;2-Y. Am J Med Genet. 1996. PMID: 8834045

5

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

6

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

7

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

8

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

9

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

10

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.

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