Brown SA - Search Results

1

Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian age.

Kline JK, Kinney AM, Levin B, Brown SA, Hadd AG, Warburton D. Kline JK, et al. Among authors: brown sa. Menopause. 2014 Jul;21(7):740-8. doi: 10.1097/GME.0000000000000139. Menopause. 2014. PMID: 24423935 Free PMC article.

2

Skewed X chromosome inactivation and trisomic spontaneous abortion: no association.

Warburton D, Kline J, Kinney A, Yu CY, Levin B, Brown S. Warburton D, et al. Am J Hum Genet. 2009 Aug;85(2):179-93. doi: 10.1016/j.ajhg.2009.07.002. Epub 2009 Jul 30. Am J Hum Genet. 2009. PMID: 19646676 Free PMC article.

3

X-chromosome inactivation and ovarian age during the reproductive years.

Kline J, Kinney A, Levin B, Kelly A, Yu CY, Brown S, Warburton D. Kline J, et al. Fertil Steril. 2006 May;85(5):1488-95. doi: 10.1016/j.fertnstert.2005.10.059. Fertil Steril. 2006. PMID: 16647378 Free article. Clinical Trial.

4

Trisomic pregnancy and intermediate CGG repeat length at the FMR1 locus.

Kline J, Kinney A, Brown S, Levin B, Oppenheimer K, Warburton D. Kline J, et al. Hum Reprod. 2012 Jul;27(7):2224-32. doi: 10.1093/humrep/des098. Epub 2012 Apr 6. Hum Reprod. 2012. PMID: 22493044 Free PMC article.

5

Using FISH to increase the yield and accuracy of karyotypes from spontaneous abortion specimens.

Jobanputra V, Esteves C, Sobrino A, Brown S, Kline J, Warburton D. Jobanputra V, et al. Prenat Diagn. 2011 Aug;31(8):755-9. doi: 10.1002/pd.2759. Epub 2011 Apr 11. Prenat Diagn. 2011. PMID: 21484844 Free PMC article.

6

Copy number changes on the X chromosome in women with and without highly skewed X-chromosome inactivation.

Jobanputra V, Levy B, Kinney A, Brown S, Shirazi M, Yu C, Kline J, Warburton D. Jobanputra V, et al. Cytogenet Genome Res. 2012;136(4):264-9. doi: 10.1159/000337920. Epub 2012 Apr 20. Cytogenet Genome Res. 2012. PMID: 22516899 Free PMC article.

7

Validation of QF-PCR for prenatal aneuploidy screening in the United States.

Brown L, Abigania M, Warburton D, Brown S. Brown L, et al. Prenat Diagn. 2006 Nov;26(11):1068-74. doi: 10.1002/pd.1558. Prenat Diagn. 2006. PMID: 16952193

8

Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.

Brown S, Gersen S, Anyane-Yeboa K, Warburton D. Brown S, et al. Am J Med Genet. 1993 Jan 1;45(1):52-9. doi: 10.1002/ajmg.1320450115. Am J Med Genet. 1993. PMID: 8418661 Review.

9

The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32.

Brown S, Russo J, Chitayat D, Warburton D. Brown S, et al. Am J Hum Genet. 1995 Oct;57(4):859-66. Am J Hum Genet. 1995. PMID: 7573047 Free PMC article.

10

Duplication of the ZIC2 gene is not associated with holoprosencephaly.

Jobanputra V, Burke A, Kwame AY, Shanmugham A, Shirazi M, Brown S, Warburton PE, Levy B, Warburton D. Jobanputra V, et al. Am J Med Genet A. 2012 Jan;158A(1):103-8. doi: 10.1002/ajmg.a.34375. Epub 2011 Nov 21. Am J Med Genet A. 2012. PMID: 22105922 Free PMC article.

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