Cargile CB - Search Results

1

Chromosome microdissection identifies cryptic sites of DNA sequence amplification in human ovarian carcinoma.

Guan XY, Cargile CB, Anzick SL, Thompson FH, Meltzer PS, Bittner ML, Taetle R, McGill JR, Trent JM. Guan XY, et al. Among authors: cargile cb. Cancer Res. 1995 Aug 1;55(15):3380-5. Cancer Res. 1995. PMID: 7614475

2

PTEN mutations and microsatellite instability in complex atypical hyperplasia, a precursor lesion to uterine endometrioid carcinoma.

Levine RL, Cargile CB, Blazes MS, van Rees B, Kurman RJ, Ellenson LH. Levine RL, et al. Among authors: cargile cb. Cancer Res. 1998 Aug 1;58(15):3254-8. Cancer Res. 1998. PMID: 9699651

3

Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.

Cargile CB, Goh DL, Goodman BK, Chen XN, Korenberg JR, Semenza GL, Thomas GH. Cargile CB, et al. Am J Med Genet. 2002 Apr 22;109(2):133-8. doi: 10.1002/ajmg.10323. Am J Med Genet. 2002. PMID: 11977162

4

Facial dysgenesis: a novel facial syndrome with chromosome 7 deletion p15.1-21.1.

Hoover-Fong JE, Cai J, Cargile CB, Thomas GH, Patel A, Griffin CA, Jabs EW, Hamosh A. Hoover-Fong JE, et al. Among authors: cargile cb. Am J Med Genet A. 2003 Feb 15;117A(1):47-56. doi: 10.1002/ajmg.a.10046. Am J Med Genet A. 2003. PMID: 12548740

5

Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat.

Goodman BK, Stone K, Coddett JM, Cargile CB, Gurewitsch ED, Blakemore KJ, Stetten G. Goodman BK, et al. Among authors: cargile cb. Prenat Diagn. 1999 Dec;19(12):1150-6. doi: 10.1002/(sici)1097-0223(199912)19:12<1150::aid-pd733>3.0.co;2-0. Prenat Diagn. 1999. PMID: 10590434 Review.

6

Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12).

Cargile CB, McIntosh I, Clough MV, Rutberg J, Yaghmai R, Goodman BK, Chen XN, Korenberg JR, Thomas GH, Geraghty MT. Cargile CB, et al. Am J Med Genet. 2000 Jun 19;92(5):328-35. doi: 10.1002/1096-8628(20000619)92:5<328::aid-ajmg7>3.0.co;2-p. Am J Med Genet. 2000. PMID: 10861662

7

Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.

Fechner PY, Rosenberg C, Stetten G, Cargile CB, Pearson PL, Smith KD, Migeon CJ, Berkovitz GD. Fechner PY, et al. Among authors: cargile cb. Cytogenet Cell Genet. 1994;66(1):22-6. doi: 10.1159/000133656. Cytogenet Cell Genet. 1994. PMID: 8275702

8

The Barr body is a looped X chromosome formed by telomere association.

Walker CL, Cargile CB, Floy KM, Delannoy M, Migeon BR. Walker CL, et al. Among authors: cargile cb. Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6191-5. doi: 10.1073/pnas.88.14.6191. Proc Natl Acad Sci U S A. 1991. PMID: 1712482 Free PMC article.

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