Migeon B - Search Results

1

Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome.

Macpherson JN, Curtis G, Crolla JA, Dennis N, Migeon B, Grewal PK, Hirst MC, Davies KE, Jacobs PA. Macpherson JN, et al. Among authors: migeon b. J Med Genet. 1995 Mar;32(3):236-9. doi: 10.1136/jmg.32.3.236. J Med Genet. 1995. PMID: 7783179 Free PMC article.

2

Studies of X-chromosome inactivation in trisomies.

Jacobs PA, Migeon BR. Jacobs PA, et al. Among authors: migeon br. Cytogenet Cell Genet. 1989;50(2-3):75-7. doi: 10.1159/000132727. Cytogenet Cell Genet. 1989. PMID: 2776488

3

Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes.

Migeon BR, Luo S, Stasiowski BA, Jani M, Axelman J, Van Dyke DL, Weiss L, Jacobs PA, Yang-Feng TL, Wiley JE. Migeon BR, et al. Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):12025-9. doi: 10.1073/pnas.90.24.12025. Proc Natl Acad Sci U S A. 1993. PMID: 8265665 Free PMC article.

4

Concerning the role of X-inactivation and DNA methylation in fragile X syndrome.

Migeon BR. Migeon BR. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):291-8. doi: 10.1002/ajmg.1320430145. Am J Med Genet. 1992. PMID: 1605203 Review.

5

X inactivation in triploidy and trisomy: the search for autosomal transfactors that choose the active X.

Migeon BR, Pappas K, Stetten G, Trunca C, Jacobs PA. Migeon BR, et al. Eur J Hum Genet. 2008 Feb;16(2):153-62. doi: 10.1038/sj.ejhg.5201944. Epub 2007 Oct 31. Eur J Hum Genet. 2008. PMID: 17971834

6

DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late.

Torchia BS, Call LM, Migeon BR. Torchia BS, et al. Among authors: migeon br. Am J Hum Genet. 1994 Jul;55(1):96-104. Am J Hum Genet. 1994. PMID: 8023856 Free PMC article.

7

NICHD conference. Role of DNA methylation in X inactivation and the fragile X syndrome.

Migeon BR. Migeon BR. Am J Med Genet. 1993 Jul 1;46(6):685-6. doi: 10.1002/ajmg.1320460617. Am J Med Genet. 1993. PMID: 8103290 No abstract available.

8

Mechanism of origin of complete hydatidiform moles.

Jacobs PA, Wilson CM, Sprenkle JA, Rosenshein NB, Migeon BR. Jacobs PA, et al. Among authors: migeon br. Nature. 1980 Aug 14;286(5774):714-6. doi: 10.1038/286714a0. Nature. 1980. PMID: 6447836

9

Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.

Migeon BR, Dunn MA, Thomas G, Schmeckpeper BJ, Naidu S. Migeon BR, et al. Am J Hum Genet. 1995 Mar;56(3):647-53. Am J Hum Genet. 1995. PMID: 7887418 Free PMC article.

10

DNA methylation of the fragile X locus in somatic and germ cells during fetal development: relevance to the fragile X syndrome and X inactivation.

Luo S, Robinson JC, Reiss AL, Migeon BR. Luo S, et al. Among authors: migeon br. Somat Cell Mol Genet. 1993 Jul;19(4):393-404. doi: 10.1007/BF01232750. Somat Cell Mol Genet. 1993. PMID: 8211380

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