Zobrazeno 1 - 10
of 203
pro vyhledávání: '"ROBINOW, M"'
Autor:
Robinow M
Publikováno v:
Clinical Dysmorphology. 2:189
The history of the Robinow (fetal face) syndrome and the evolution of the phenotype are presented. Non-specific and syndrome-specific abnormalities are listed, discussed and illustrated. Existence of an autosomal dominant and an autosomal recessive t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21f27fb9e6a62b7672738c8732ab08a0
https://doi.org/10.1097/00019605-199307000-00001
https://doi.org/10.1097/00019605-199307000-00001
Publikováno v:
Humangenetik (00187348); 1974, Vol. 25 Issue 1, p69-78, 10p
Publikováno v:
Journal of Medical Genetics; Feb1983, Vol. 20 Issue 1, p1-11, 11p, 10 Charts
Publikováno v:
Human Genetics; March 1974, Vol. 25 Issue: 1 p69-78, 10p
Autor:
ROBINOW, M., HAMILTON, W. F.
Publikováno v:
American Journal of Diseases of Children; October 1940, Vol. 60 Issue: 4 p827-840, 14p
Autor:
ROBINOW, M.
Publikováno v:
American Journal of Diseases of Children; August 1942, Vol. 64 Issue: 2 p229-236, 8p
Publikováno v:
American Journal of Diseases of Children; July 1939, Vol. 58 Issue: 1 p102-118, 17p
Autor:
ROBINOW, M, SILVERMAN, F N
Publikováno v:
Pediatrics; November 1957, Vol. 20 Issue: 5 p921-940, 20p
Publikováno v:
Pediatrics; April 1953, Vol. 11 Issue: 4 p309-322, 14p
Nine related individuals have been identified as being trisomic for the distal part of the long arm of chromosome 15 (15q23 to 15qter). The physical characteristics, especially the facial features, of these nine cases are similar and distinctive. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95e1b81298903240bb03a2c5e000c339
https://europepmc.org/articles/PMC1684424/
https://europepmc.org/articles/PMC1684424/
