Migeon C - Search Results

1

Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development.

Mardo V, Squibb EE, Braverman N, Hoover-Fong JE, Migeon C, Batista DA, Thomas GH. Mardo V, et al. Among authors: migeon c. Am J Med Genet A. 2008 Sep 1;146A(17):2293-7. doi: 10.1002/ajmg.a.32316. Am J Med Genet A. 2008. PMID: 18661548 No abstract available.

2

Embryonic testicular regression sequence: a part of the clinical spectrum of 46,XY gonadal dysgenesis.

Marcantonio SM, Fechner PY, Migeon CJ, Perlman EJ, Berkovitz GD. Marcantonio SM, et al. Among authors: migeon cj. Am J Med Genet. 1994 Jan 1;49(1):1-5. doi: 10.1002/ajmg.1320490102. Am J Med Genet. 1994. PMID: 8172233

3

Partial gonadal dysgenesis in a patient with a marker Y chromosome.

Fechner PY, Smith KD, Jabs EW, Migeon CJ, Berkovitz GD. Fechner PY, et al. Among authors: migeon cj. Am J Med Genet. 1992 Apr 1;42(6):807-12. doi: 10.1002/ajmg.1320420612. Am J Med Genet. 1992. PMID: 1313209

4

Abnormal gonadal differentiation in two subjects with ambiguous genitalia, Mullerian structures, and normally developed testes: evidence for a defect in gonadal ridge development.

Fuqua JS, Sher ES, Perlman EJ, Urban MD, Ghahremani M, Pelletier J, Migeon CJ, Brown TR, Berkovitz GD. Fuqua JS, et al. Among authors: migeon cj. Hum Genet. 1996 Apr;97(4):506-11. doi: 10.1007/BF02267076. Hum Genet. 1996. PMID: 8834252

5

The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism.

Berkovitz GD, Fechner PY, Marcantonio SM, Bland G, Stetten G, Goodfellow PN, Smith KD, Migeon CJ. Berkovitz GD, et al. Among authors: migeon cj. Hum Genet. 1992 Feb;88(4):411-6. doi: 10.1007/BF00215675. Hum Genet. 1992. PMID: 1740318

6

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: migeon cj. Cytogenet Cell Genet. 1994;66(1):22-6. doi: 10.1159/000133656. Cytogenet Cell Genet. 1994. PMID: 8275702

7

Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndrome.

Brown TR, Lubahn DB, Wilson EM, Joseph DR, French FS, Migeon CJ. Brown TR, et al. Among authors: migeon cj. Proc Natl Acad Sci U S A. 1988 Nov;85(21):8151-5. doi: 10.1073/pnas.85.21.8151. Proc Natl Acad Sci U S A. 1988. PMID: 3186717 Free PMC article.

8

Vaginal reconstruction after initial construction of the external genitalia in girls with salt-wasting adrenal hyperplasia.

Bailez MM, Gearhart JP, Migeon C, Rock J. Bailez MM, et al. Among authors: migeon c. J Urol. 1992 Aug;148(2 Pt 2):680-2; discussion 683-4. doi: 10.1016/s0022-5347(17)36691-0. J Urol. 1992. PMID: 1640545 Free article.

9

The role of the sex-determining region Y gene in the etiology of 46,XX maleness.

Fechner PY, Marcantonio SM, Jaswaney V, Stetten G, Goodfellow PN, Migeon CJ, Smith KD, Berkovitz GD, Amrhein JA, Bard PA, et al. Fechner PY, et al. Among authors: migeon cj. J Clin Endocrinol Metab. 1993 Mar;76(3):690-5. doi: 10.1210/jcem.76.3.8383144. J Clin Endocrinol Metab. 1993. PMID: 8383144

10

Evaluation of boys with marked breast development at puberty.

Sher ES, Migeon CJ, Berkovitz GD. Sher ES, et al. Among authors: migeon cj. Clin Pediatr (Phila). 1998 Jun;37(6):367-71. doi: 10.1177/000992289803700606. Clin Pediatr (Phila). 1998. PMID: 9637901 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

365 results

Search Page

Filters