Zobrazeno 1 - 2
of 2
pro vyhledávání: '"N A, Posch"'
Autor:
R J, Galjaard, L I, van der Ham, N A, Posch, P F, Dijkstra, B A, Oostra, S E, Hovius, E J, Timmenga, G J, Sonneveld, A J, Hoogeboom, P, Heutink
Publikováno v:
American journal of medical genetics. 98(3)
Hereditary isolated brachydactyly type C (OMIM 113100) mostly follows an autosomal dominant pattern of inheritance with a marked variability in expression. This phenotype has been mapped to two different loci on chromosomes 12q24 and 20q11.2. The lat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b877333f2bdaba81ea2aa5ab0773c13e
https://pubmed.ncbi.nlm.nih.gov/11169564
https://pubmed.ncbi.nlm.nih.gov/11169564
Autor:
J, Bel Comos, A, Ribera Crusafont, A, Natal Pujol, W, Coroleu Lletget, N, Pujol Posch, J, Prats Viñas
Publikováno v:
Anales espanoles de pediatria. 35(4)
We studied the ABO haemolytic disease of the newborn in our neonatal unit to consider their serological aspects and clinical importance. 21% of all pregnancies were ABO incompatibles. The direct antiglobulin test was positive in 46 (11.3%) of them. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7854facf71fe2ae8a5d06e84480ac64
https://pubmed.ncbi.nlm.nih.gov/1763851
https://pubmed.ncbi.nlm.nih.gov/1763851