Zobrazeno 1 - 10
of 224
pro vyhledávání: '"Gail H Vance"'
Autor:
Joshua L. Deignan, Vimla Aggarwal, Allen E. Bale, Daniel B. Bellissimo, Jessica K. Booker, Yang Cao, Kristy R. Crooks, Kristen L. Deak, Daniela Del Gaudio, Birgit Funke, Nicole L. Hoppman, Vanessa Horner, Robert B. Hufnagel, Colleen Jackson-Cook, Prasad Koduru, Marco L. Leung, Shibo Li, Pengfei Liu, Minjie Luo, Rong Mao, Heather Mason-Suares, Fady M. Mikhail, Stephen R. Moore, Rizwan C. Naeem, Laura M. Pollard, Elena A. Repnikova, Lina Shao, Brandon M. Shaw, Shashirekha Shetty, Teresa A. Smolarek, Elizabeth Spiteri, Jessica Van Ziffle, Gail H. Vance, Cindy L. Vnencak-Jones, Eli S. Williams
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101820- (2024)
Purpose: The specialty of Laboratory Genetics and Genomics (LGG) was created in 2017 in an effort to reflect the increasing convergence in technologies and approaches between clinical molecular genetics and clinical cytogenetics. However, there has n
Externí odkaz:
https://doaj.org/article/06de2e3b5f9244b89cae6954ab35c034
Autor:
Hart, Curtis W.
Publikováno v:
Journal of Religion and Health, 1999 Apr 01. 38(1), 79-80.
Externí odkaz:
https://www.jstor.org/stable/27511327
Publikováno v:
BMJ case reports. 15(7)
Malignant gastrointestinal neuroectodermal tumour (GNET) is a rare, aggressive neoplasm with fewer than 100 cases reported in the literature. Most cases arise in the tubular gastrointestinal tract. We reported a unique case of GNET arising in the ext
Autor:
Susan Cordes Selby, Aiko Iwata‐Otsubo, Paula Delk, Todd D. Nebesio, Anisha Gohil, Peggy Matlock, Wilfredo Torres‐Martinez, Gail H. Vance
Publikováno v:
Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Abstract Two siblings with the same male unbalanced karyotype demonstrate sex reversal. The older sib appeared phenotypically female and the younger sib demonstrated a male gender. The female had gonadal dysgenesis with bilateral ovatestes. The male
Externí odkaz:
https://doaj.org/article/9da54e73e68c45589db4a69c9f44ea8d
Autor:
Gail H, Vance, Wahab A, Khan
Publikováno v:
Clinics in Laboratory Medicine. 42:573-586
Publikováno v:
Case Reports in Genetics, Vol 2020 (2020)
We report on a 12-year-old female with both a partial duplication and deletion involving chromosome 6. The duplication involves 6p25.3p24.3 (7.585 Mb) while the deletion includes 6q27q27 (6.244 Mb). This chromosomal abnormality is also described as d
Externí odkaz:
https://doaj.org/article/f6c4fd36e13b4a4d9b310ed1eced7af1
Autor:
Margaret E. Armstrong, David D. Weaver, Melissa D. Lah, Gail H. Vance, Benjamin J. Landis, Stephanie M. Ware, Benjamin M. Helm
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Abstract Background Supernumerary marker chromosomes derived from chromosome 5 (SMC5) and 5p13 duplication syndrome are rare disorders, and phenotypic descriptions of patients are necessary to better define genotype-phenotype correlations for accurat
Externí odkaz:
https://doaj.org/article/c2f6926b75584a169aec0e6ed77b3a2d
Publikováno v:
Journal of Genetic Counseling.
Publikováno v:
Journal of Cutaneous Pathology. 49:808-812
Autor:
Gail H Vance, Teresa Lotodo, Nicholas Kigen, Ryan Stohler, Haki Choi, Festus Njuguna, Ann M Moormann, Erastus Kirwa, Sandra Langat, Patrick Loehrer, Terry Vik
Publikováno v:
ecancermedicalscience. 17