Batista DA - Search Results

1

Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.

Chen H, Tuck-Muller CM, Batista DA, Wertelecki W. Chen H, et al. Among authors: batista da. Am J Med Genet. 1995 Mar 27;56(2):219-33. doi: 10.1002/ajmg.1320560221. Am J Med Genet. 1995. PMID: 7625449 Review.

2

Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature.

Tuck-Muller CM, Chen H, Martínez JE, Shen CC, Li S, Kusyk C, Batista DA, Bhatnagar YM, Dowling E, Wertelecki W. Tuck-Muller CM, et al. Among authors: batista da. Hum Genet. 1995 Jul;96(1):119-29. doi: 10.1007/BF00214200. Hum Genet. 1995. PMID: 7607645 Review.

3

Duplication of the short arm of the X chromosome in mother and daughter.

Tuck-Muller CM, Martinez JE, Batista DA, Kearns WG, Wertelecki W. Tuck-Muller CM, et al. Among authors: batista da. Hum Genet. 1993 May;91(4):395-400. doi: 10.1007/BF00217366. Hum Genet. 1993. PMID: 8500796 Review.

4

A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization.

Batista DA, Tuck-Muller CM, Martinez JE, Kearns WG, Pearson PL, Stetten G. Batista DA, et al. Hum Genet. 1993 Sep;92(2):117-21. doi: 10.1007/BF00219677. Hum Genet. 1993. PMID: 8370575

5

Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.

Batista DA, Pai GS, Stetten G. Batista DA, et al. Am J Med Genet. 1994 Nov 15;53(3):255-63. doi: 10.1002/ajmg.1320530311. Am J Med Genet. 1994. PMID: 7856662 Review.

6

Tetrasomy 18p: tentative delineation of a syndrome.

Batista DA, Vianna-Morgante AM, Richieri-Costa A. Batista DA, et al. J Med Genet. 1983 Apr;20(2):144-7. doi: 10.1136/jmg.20.2.144. J Med Genet. 1983. PMID: 6842551 Free PMC article.

7

Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins.

Doheny KF, Rasmussen SA, Rutberg J, Semenza GL, Stamberg J, Schwartz M, Batista DA, Stetten G, Thomas GH. Doheny KF, et al. Among authors: batista da. Am J Med Genet. 1997 Mar 17;69(2):188-93. Am J Med Genet. 1997. PMID: 9056559

8

Mosaic trisomy 13: understanding origin using SNP array.

Jinawath N, Zambrano R, Wohler E, Palmquist MK, Hoover-Fong J, Hamosh A, Batista DA. Jinawath N, et al. Among authors: batista da. J Med Genet. 2011 May;48(5):323-6. doi: 10.1136/jmg.2010.083931. Epub 2010 Nov 19. J Med Genet. 2011. PMID: 21097773

9

Unbalanced translocation 9;16 in two children with dysmorphic features, and severe developmental delay: Evidence of cross-over within derivative chromosome 9 in patient #1.

Zambrano RM, Wohler E, Annerén G, Thuresson AC, Cutting GR, Batista DA. Zambrano RM, et al. Among authors: batista da. Eur J Med Genet. 2011 Mar-Apr;54(2):189-93. doi: 10.1016/j.ejmg.2010.11.008. Epub 2010 Dec 7. Eur J Med Genet. 2011. PMID: 21144914

10

Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

Li F, Shen Y, Köhler U, Sharkey FH, Menon D, Coulleaux L, Malan V, Rio M, McMullan DJ, Cox H, Fagan KA, Gaunt L, Metcalfe K, Heinrich U, Hislop G, Maye U, Sutcliffe M, Wu BL, Thiel BD, Mulchandani S, Conlin LK, Spinner NB, Murphy KM, Batista DA. Li F, et al. Among authors: batista da. Eur J Med Genet. 2010 Mar-Apr;53(2):93-9. doi: 10.1016/j.ejmg.2010.01.004. Epub 2010 Feb 2. Eur J Med Genet. 2010. PMID: 20132918

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