Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Hymie Gordon"'
Publikováno v:
Clinical Genetics. 8:149-160
The karyotype 46,XX/69,XXY was found in a 13-year-old mentally subnormal patient with club feet, strabismus, eunuchoid habitus, small penis, midscrotal urethrovaginal opening, small descended left testis, and small undescended right testis; no ovaria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76f1db47571f716536b48395216bd3e6
https://doi.org/10.1111/j.1399-0004.1975.tb04403.x
https://doi.org/10.1111/j.1399-0004.1975.tb04403.x
Publikováno v:
American Journal of Medical Genetics. 36:333-335
Most structural congenital heart defects (CHD) are thought to be multifactorially determined, but the precise causal factors usually are unknown. One may postulate that vascular events, such as hemorrhage in the developing embryo, could influence mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2c9fcb11bfa5a56b88dd9f8aa3291e2
https://doi.org/10.1002/ajmg.1320360318
https://doi.org/10.1002/ajmg.1320360318
Publikováno v:
Journal of neurosurgery. 74(6)
✓ Spontaneous bilateral carotid-cavernous fistulae and cervical artery dissection is reported in a 20-year-old woman with Ehlers-Danlos syndrome Type IV. The clinical features of 16 previously published cases of spontaneous carotid-cavernous fistul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c408363b9a286008c22d9a80ca695f3
https://pubmed.ncbi.nlm.nih.gov/2033461
https://pubmed.ncbi.nlm.nih.gov/2033461
Publikováno v:
Clinical Genetics. 24:462-462
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36dc36c3f4b1eb1662c9e1f7953a91c9
https://doi.org/10.1111/j.1399-0004.1983.tb00105.x
https://doi.org/10.1111/j.1399-0004.1983.tb00105.x
Autor:
Hymie Gordon
Publikováno v:
Mayo Clinic Proceedings. 70:510-511
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d70d38f2d9c7f91e70fe76efd2ae334
https://doi.org/10.4065/70.5.510-a
https://doi.org/10.4065/70.5.510-a
Publikováno v:
Medicine. 64:270-283
Of 40 patients (16 males and 24 females), 29 had cardiac myxoma(s), 14 had skin pigmentation (lentigo and several types of nevi) which also commonly affected the lips, 6 had skin myxoma(s), and 12 had both pigmentation and myxoma(s); 18 had primary p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06131c1e53bf9d92b36ee3afbe701585
https://doi.org/10.1097/00005792-198507000-00007
https://doi.org/10.1097/00005792-198507000-00007
Autor:
Virginia V. Michels, Stephen N. Thibodeau, Hymie Gordon, Edward J. O'connell, Daniel J. Schaid, Laura A. Cummins, D. Brian Dawson
Publikováno v:
Mayo Clinic Proceedings. 64:325-334
As a result of recent advances in molecular genetics, carrier testing for cystic fibrosis (CF) is now available as a clinical assay in a limited number of laboratories. Because neither the gene nor the mutation for this disorder has yet been defined,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97ff9a5e86858a33cc49c90a38e3e141
https://doi.org/10.1016/s0025-6196(12)65252-5
https://doi.org/10.1016/s0025-6196(12)65252-5
Autor:
John T. McCall, William P. Baldus, Archie H. Baggenstoss, Howard F. Taswell, Gene LeSage, S. Breanndan Moore, Hymie Gordon, Virgil F. Fairbanks
Publikováno v:
Gastroenterology. 84:1471-1477
To evaluate the roles of alcohol and genetic factors in hepatic iron overload, we studied prospectively 61 patients selected solely on the basis of increased stainable hepatic iron (grade 3 or 4). Independent comparisons were made between alcoholic (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1c2b9e36f1b4a83a6525562cbe74ea6
https://doi.org/10.1016/0016-5085(83)90367-0
https://doi.org/10.1016/0016-5085(83)90367-0
Publikováno v:
Mayo Clinic Proceedings. 62:558-567
Cardiac myxomas from eight patients were examined cytogenetically in short-term cultures. Cultures could not be established in two of the eight cases. Chromosomally abnormal clones occurred in two of the myxomas; their karyotypes were 45,X,-Y,+7,-18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bb15e4f1c18703a5eb725fffd299395
https://doi.org/10.1016/s0025-6196(12)62293-9
https://doi.org/10.1016/s0025-6196(12)62293-9
Publikováno v:
Mayo Clinic Proceedings. 62:589-594
The Marfan syndrome, a generalized inherited disorder, is usually diagnosed in young patients and is associated with a poor prognosis. With use of our diagnostic-retrieval system, we identified 28 patients with the Marfan syndrome who were 32 years o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25f2948217bb75950956c67d1c5c20d2
https://doi.org/10.1016/s0025-6196(12)62297-6
https://doi.org/10.1016/s0025-6196(12)62297-6