Pericentric inversion of chromosome 19: prenatal diagnosis and genetic counselling.

Autor: Tharapel, Avirachan T., Ward, Jewell C., Wiggins, Lee, Wilroy, R. Sid, Tharapel, A T, Ward, J C, Wiggins, L, Wilroy, R S Jr

Publikováno v: Prenatal Diagnosis; Jan1986, Vol. 6 Issue 1, p75-78, 4p

Chromosome duplications and deletions and their mechanisms of origin.

Autor: Tharapel AT; Departments of Pediatrics, Obstetrics, and Gynecology, The University of Tennessee Health Sciences Center, Memphis, TN, USA. atharapel@utmem1.utmem.edu, Michaelis RC, Velagaleti GV, Laundon CH, Martens PR, Buchanan PD, Teague KE, Tharapel SA, Wilroy RS Jr

Publikováno v: Cytogenetics and cell genetics [Cytogenet Cell Genet] 1999; Vol. 85 (3-4), pp. 285-90.

Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization.

Autor: Zhao J; Department of Pediatrics, University of Tennessee, Memphis, USA., Gordon PL, Wilroy RS Jr, Martens PR, Tarleton J, Shulman LP, Simpson JL, Elias S, Tharapel AT

Publikováno v: American journal of medical genetics [Am J Med Genet] 1995 May 08; Vol. 56 (4), pp. 398-402.

Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.

Autor: Tharapel AT; Department of Pediatrics, University of Tennessee, Memphis 38163., Qumsiyeh MB, Martens PR, Tharapel SA, Dalton JD, Ward JC, Wilroy RS Jr

Publikováno v: American journal of medical genetics [Am J Med Genet] 1991 Jul 01; Vol. 40 (1), pp. 117-20.

X-autosome translocation in normal mother and effectively 21-monosomic daughter.

Autor: Summitt RL, Martens PR, Wilroy RS Jr

Publikováno v: The Journal of pediatrics [J Pediatr] 1974 Apr; Vol. 84 (4), pp. 539-46.