Zobrazeno 1 - 10
of 19
pro vyhledávání: '"C F, Salinas"'
Publikováno v:
Acta Paediatrica. 80:93-95
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf5eb7e4b34f238a9eb6140b0a8a99be
https://doi.org/10.1111/j.1651-2227.1991.tb11736.x
https://doi.org/10.1111/j.1651-2227.1991.tb11736.x
Publikováno v:
American journal of medical genetics. 64(3)
Seckel syndrome is a rare, recessively inherited disorder of severe growth retardation and distinct craniofacial, orodental, and skeletal anomalies. Even though there are well-established minimum diagnostic criteria for this syndrome, controversy exi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0b1631a95b30012003ee8681ff8b83bd
https://pubmed.ncbi.nlm.nih.gov/9182792
https://pubmed.ncbi.nlm.nih.gov/9182792
Publikováno v:
Pediatrics. 69(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e0c4ecfa72f14060783def2e89d9841
https://pubmed.ncbi.nlm.nih.gov/7079011
https://pubmed.ncbi.nlm.nih.gov/7079011
Publikováno v:
American journal of diseases of children (1960). 133(5)
In two unrelated families, there was familial occurrence of gastroschisis. In one family, a boy and girl were affected and there was a family history of stillbirth, abortion, prematurity, and esophageal obstruction. In the second family, two boys wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e2cb4396b9310ac54f6959ef6388d96b
https://pubmed.ncbi.nlm.nih.gov/155396
https://pubmed.ncbi.nlm.nih.gov/155396
Publikováno v:
Birth defects original article series. 15(5B)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6655d03d784d8824c85a1d5d2b77f45
https://pubmed.ncbi.nlm.nih.gov/526587
https://pubmed.ncbi.nlm.nih.gov/526587
Autor:
G N, Coston, C F, Salinas
Publikováno v:
Birth defects original article series. 24(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7042ec02a506710208fddc394828ceaa
https://pubmed.ncbi.nlm.nih.gov/3179428
https://pubmed.ncbi.nlm.nih.gov/3179428
Publikováno v:
Birth defects original article series. 12(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0a9c8a64dcddccab07fc49a79b352d4c
https://pubmed.ncbi.nlm.nih.gov/953233
https://pubmed.ncbi.nlm.nih.gov/953233
Publikováno v:
Birth defects original article series. 24(2)
A study of density of sweat pores in 594 individuals indicated that the average number of pores per cm2 in the hypothenar area was 490.4 for white newborns, 513.6 for black newborns, 652.4 for white children, 629.2 for black children, 519.6 for white
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4f63950764d01bf1a0d549661c1b8e4d
https://pubmed.ncbi.nlm.nih.gov/3179435
https://pubmed.ncbi.nlm.nih.gov/3179435
Publikováno v:
Journal of craniofacial genetics and developmental biology. 2(2)
The frequency of taurodontism was studied in 1074 black children from an inner city population. Based on the index that was developed, 4.37% of the sample were determined to be affected. The frequency of taurodontism was compared to other studies. Fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::07fdd0fccf23e41443da0068d772952b
https://pubmed.ncbi.nlm.nih.gov/7174775
https://pubmed.ncbi.nlm.nih.gov/7174775
Autor:
C F, Salinas
Publikováno v:
Birth defects original article series. 16(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7cfdbc1035a3fd9e2289f756a91b6f7c
https://pubmed.ncbi.nlm.nih.gov/7448378
https://pubmed.ncbi.nlm.nih.gov/7448378