Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tammy Stump"'
Autor:
Yelena P. Wu, Elise K. Brunsgaard, Nic Siniscalchi, Tammy Stump, Heather Smith, Douglas Grossman, Jakob Jensen, David B. Buller, Jennifer L. Hay, Jincheng Shen, Benjamin A. Haaland, Kenneth P. Tercyak
Publikováno v:
Contemporary Clinical Trials Communications, Vol 42, Iss , Pp 101399- (2024)
Schools provide an ideal setting for delivery of disease prevention programs due to the ability to deliver health education and counseling, including health behavior interventions, to large numbers of students. However, the remote and hybrid learning
Externí odkaz:
https://doaj.org/article/9e5207ec385a467baac150fde5f2fe1f
Autor:
Carolyn A. Felix, Caroline S. Kim, Maureen D. Megonigal, Diana J. Slater, Douglas H. Jones, Nancy B. Spinner, Tammy Stump, Matthew R. Hosler, Peter C. Nowell, Beverly J. Lange, Eric F. Rappaport
Publikováno v:
Blood. 90:4679-4686
We used a new approach called panhandle polymerase chain reaction (PCR) to clone an MLL genomic translocation breakpoint in a case of acute lymphoblastic leukemia of infancy in which karyotype analysis was technically unsuccessful and did not show th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f9dbe46a10120959031aa149db54b87
https://doi.org/10.1182/blood.v90.12.4679.4679_4679_4686
https://doi.org/10.1182/blood.v90.12.4679.4679_4679_4686
Autor:
Elaine H. Zackai, Tammy Stump, Rhonda E. Schnur, Nancy B. Spinner, Kimberly Grace, Gordon Strathdee, Joan Overhauser, Joan E. Pellegrino, Leslie Boghosian-Sell
Publikováno v:
Human genetics. 97(4)
The ablepharon-macrostomia (AMS) and Barher-Say syndromes (BSS) are rare disorders characterized by absence of the eyelids or ectropion, macrostomia, ambiguous genitalia, abnormal ears, rudimentary nipples, and dry, redundant skin. Patients with Barb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de5b9dd025172c225ec5fa5231381310
https://pubmed.ncbi.nlm.nih.gov/8834257
https://pubmed.ncbi.nlm.nih.gov/8834257
Autor:
Nancy C. Rose, Rhonda E. Schnur, Donna M. McDonald-McGinn, Beverly S. Emanuel, Elaine H. Zackai, Laird G. Jackson, Sheryl J. Menacker, Tammy Stump
Publikováno v:
American journal of medical genetics. 42(5)
We describe a boy with an interstitial deletion of 6(q13-q15) and include "coarse" facial features, upslanting palpebral fissures, thin vermilion border of the upper lip, elongated philtrum, developmental delay, and profound hypotonia. The child's ey
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3841954ad3a7f73439de32e8174fd66a
https://pubmed.ncbi.nlm.nih.gov/1632442
https://pubmed.ncbi.nlm.nih.gov/1632442