Zobrazeno 1 - 10
of 115
pro vyhledávání: '"John L. Hamerton"'
Publikováno v:
Classification and Human Evolution ISBN: 9781315081083
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87321f7c170f902a71501b85b84a9044
https://doi.org/10.4324/9781315081083-11
https://doi.org/10.4324/9781315081083-11
Publikováno v:
Clinical Genetics. 14:50-54
Cultured skin fibroblasts from patients with Duchenne muscular dystrophy were studied with a double-labeling procedure. Preliminary evaluation of the growth characteristics and average viability of dystrophic cells did not show any major abnormalitie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5fdc0ff0f56a09136fd8450a8d73a44
https://doi.org/10.1111/j.1399-0004.1978.tb02060.x
https://doi.org/10.1111/j.1399-0004.1978.tb02060.x
Publikováno v:
Prenatal Diagnosis. 14:1253-1265
This paper presents the results of a detailed study of the genetic prenatal diagnostic services available in Canada in 1990. All 22 genetic centres offering prenatal diagnostic services as well as the 64 laboratories processing samples were surveyed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c90a0a469aa3aa4caa97e6b3e20c230
https://doi.org/10.1002/pd.1970141310
https://doi.org/10.1002/pd.1970141310
Autor:
Barbara McGillivray, Albert E. Chudley, John L. Hamerton, A. J. Kirkilionis, D. L. Yan, Cheryl R. Greenberg
Publikováno v:
American Journal of Medical Genetics. 43:588-591
We report on a family showing transmission of the fra(X) gene by 3 nonpenetrant, fra(X) negative, normally intelligent, full and half-brothers to their affected grandsons. The mothers of the affected boys are obligate carriers, fra(X) negative, and o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::204947cda79e3eb599e64c12c6dea5be
https://doi.org/10.1002/ajmg.1320430316
https://doi.org/10.1002/ajmg.1320430316
Publikováno v:
Prenatal Diagnosis. 12:473-476
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26d7729fbe8106f9f42ea3de55c982da
https://doi.org/10.1002/pd.1970120516
https://doi.org/10.1002/pd.1970120516
Publikováno v:
American Journal of Medical Genetics. 40:454-459
The Prader-Willi (PWS) and Angelman syndromes (AS) share the same apparent cytogenetic and molecular lesions of 15q11-13 and yet exhibit distinct clinical phenotypes. The etiology of PWS or AS appears to depend on the parental origin of the aberrant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a653e3a35d1f27f720fbe411373edf98
https://doi.org/10.1002/ajmg.1320400416
https://doi.org/10.1002/ajmg.1320400416
Publikováno v:
Genomics. 9:524-535
In an attempt to elucidate the relationship between genetic alterations at chromosomal bands 15q11.2–12 and the Prader-Willi syndrome (PWS), we have constructed a long-range restriction map of this region using a combination of pulsed-field gel tec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62a8e3eaf76e8c6286a88a2505169fdf
https://doi.org/10.1016/0888-7543(91)90420-j
https://doi.org/10.1016/0888-7543(91)90420-j
Autor:
John L. Hamerton, Leonie C. Stranc
Publikováno v:
Lancet (London, England). 354(9191)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f143d89651b4c8231437e916c140ac4
https://pubmed.ncbi.nlm.nih.gov/10568569
https://pubmed.ncbi.nlm.nih.gov/10568569
Publikováno v:
Lancet (London, England). 349(9053)
Prenatal procedures for the diagnosis of genetic disorders or fetal anomalies differ in their invasiveness, risks, accuracy, cost, optimal time of performance, and appropriateness for a given indication. Both midtrimester amniocentesis and chorion vi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e3b79b7b74f2344c837a92255ebc106
https://pubmed.ncbi.nlm.nih.gov/9149724
https://pubmed.ncbi.nlm.nih.gov/9149724
Publikováno v:
Prenatal diagnosis. 12(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d65cfff4425645c7f20399bde640f78
https://pubmed.ncbi.nlm.nih.gov/1523206
https://pubmed.ncbi.nlm.nih.gov/1523206