Petersen MB - 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. Hum Mol Genet. 1993 Oct;2(10):1691-5. doi: 10.1093/hmg/2.10.1691. Hum Mol Genet. 1993. PMID: 8268923

2

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.

Antonarakis SE, Petersen MB, McInnis MG, Adelsberger PA, Schinzel AA, Binkert F, Pangalos C, Raoul O, Slaugenhaupt SA, Hafez M, et al. Antonarakis SE, et al. Among authors: petersen mb. Am J Hum Genet. 1992 Mar;50(3):544-50. Am J Hum Genet. 1992. PMID: 1347192 Free PMC article.

3

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: petersen mb. Hum Mol Genet. 1994 Sep;3(9):1529-35. doi: 10.1093/hmg/3.9.1529. Hum Mol Genet. 1994. PMID: 7833907

4

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

5

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: petersen mb. Hum Mol Genet. 1997 Sep;6(9):1391-9. doi: 10.1093/hmg/6.9.1391. Hum Mol Genet. 1997. PMID: 9285774

6

Non-disjunction of chromosome 18.

Bugge M, Collins A, Petersen MB, Fisher J, Brandt C, Hertz JM, Tranebjaerg L, de Lozier-Blanchet C, Nicolaides P, Brøndum-Nielsen K, Morton N, Mikkelsen M. Bugge M, et al. Among authors: petersen mb. Hum Mol Genet. 1998 Apr;7(4):661-9. doi: 10.1093/hmg/7.4.661. Hum Mol Genet. 1998. PMID: 9499419

7

Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination.

Robinson WP, Kuchinka BD, Bernasconi F, Petersen MB, Schulze A, Brondum-Nielsen K, Christian SL, Ledbetter DH, Schinzel AA, Horsthemke B, Schuffenhauer S, Michaelis RC, Langlois S, Hassold TJ. Robinson WP, et al. Among authors: petersen mb. Hum Mol Genet. 1998 Jun;7(6):1011-9. doi: 10.1093/hmg/7.6.1011. Hum Mol Genet. 1998. PMID: 9580665 Free 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: petersen mb. Hum Mol Genet. 1998 Aug;7(8):1221-7. doi: 10.1093/hmg/7.8.1221. Hum Mol Genet. 1998. PMID: 9668162

9

Nondisjunction in trisomy 21: origin and mechanisms.

Petersen MB, Mikkelsen M. Petersen MB, et al. Cytogenet Cell Genet. 2000;91(1-4):199-203. doi: 10.1159/000056844. Cytogenet Cell Genet. 2000. PMID: 11173856 Review.

10

A 48,XXY,+21 Down syndrome patient with additional paternal X and maternal 21.

Lorda-Sanchez I, Petersen MB, Binkert F, Maechler M, Schmid W, Adelsberger PA, Antonarakis SE, Schinzel A. Lorda-Sanchez I, et al. Among authors: petersen mb. Hum Genet. 1991 May;87(1):54-6. doi: 10.1007/BF01213092. Hum Genet. 1991. PMID: 1674717

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