Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Peter Osella"'
Autor:
Aubrey Milunsky, Vijay S. Tonk, Peter Osella, Bai-Lin Wu, James Skare, B R Haddad, Herman E. Wyandt
Publikováno v:
Clinical Genetics. 48:151-155
A 4-month-old child with multiple anomalies was determined to have an interstitial deletion of chromosome 15, i.e., del(15) (q12q14). The deletion appears not to be a typical deletion of 15q12 such as seen in Angelman and Prader-Willi syndromes, but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b111d39bbca2a4a31d659e40599fd894
https://doi.org/10.1111/j.1399-0004.1995.tb04076.x
https://doi.org/10.1111/j.1399-0004.1995.tb04076.x
Publikováno v:
Cancer Genetics and Cytogenetics. 64:65-68
We report three cases of meningioma. Case 1 had a dicentric chromosome number 22 resulting in partial monosomy for a portion of the q-arm, i.e., 46,XX,idic(22)(pter→q11.2: :q11.2→pter) and 46,XX,psu dic(22)(pter→q11.2: :q11.2→pter), which was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4450b781d2e21fedc0e848932a21eb7b
https://doi.org/10.1016/0165-4608(92)90325-3
https://doi.org/10.1016/0165-4608(92)90325-3
Publikováno v:
Cancer Genetics and Cytogenetics. 59:73-78
Cytogenetic analysis was performed on the metaphase spreads obtained from primary cultures of eight squamous cell carcinomas (SCCa) of the head and neck. Despite a variety of tumor sites and clinical stages, four of eight tumors studied showed the sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8017426a06a5b83d2e3f385dac761dd
https://doi.org/10.1016/0165-4608(92)90162-2
https://doi.org/10.1016/0165-4608(92)90162-2
Autor:
Nancy L. Fisher, Peter Osella, Thomas Maker, Aubrey Milunsky, Shivanand R. Patil, Roger A. Williamson, Frederick W. Luthardt, Herman E. Wyandt, Charles Y. Kawada
Publikováno v:
Prenatal Diagnosis. 10:569-574
We report three cases of amniocentesis in which mosaicism for trisomy 12 was detected in two or more independent cultures. The parents elected to terminate the pregnancy in all three cases. Follow-up studies in two of the cases confirmed the mosaicis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ea6ee79b0ac39bd04eef377d5744a34
https://doi.org/10.1002/pd.1970100904
https://doi.org/10.1002/pd.1970100904
Publikováno v:
Cancer genetics and cytogenetics. 57(2)
Chromosome analysis of bone marrow aspirate from a 46-year-old man with acute promyelocytic leukemia (APL) revealed a variant translocation, 46,XY,t(1:15;17)(p36;q22;q21.1). The breakpoints in chromosomes 15 and 17 appear to be the same as those in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bab0580d6534be7c88925cf5c8a96e11
https://pubmed.ncbi.nlm.nih.gov/1756499
https://pubmed.ncbi.nlm.nih.gov/1756499