Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
July 1, 1986British Journal of Haematology

Molecular pathology of haemoglobin H disease in Sardinians

View Full Paper
Ask AI
Bookmark
Share

Authors

EPE. PagliettiUniversity of CagliariRGR. GalanelloUniversity of ParmaPMPaolo MoiInstitute of Genetic and Biomedical Research

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Paglietti et al. (1986) studied this question.

synapsesocial.com/papers/6a880cff5ee6e03ae3cf09fbhttps://doi.org/10.1111/j.1365-2141.1986.tb07525.x
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1alpha-Thalassaemia in Sardinian infants.1980 · 4 citations
  2. 2Direct detection of the common Mediterranean beta-thalassemia gene with synthetic DNA probes. An alternative approach for prenatal diagnosis.1983 · 137 citations
  3. 3Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.1980 · 269 citations
  4. 4Highly variable regions of DNA flank the human α globin genes1981 · 169 citations
  5. 5Prenatal Diagnosis of β-Thalassemia1983 · 193 citations