טוען...
Search for consanguinity within and among families of patients with trichothiodystrophy associated with xeroderma pigmentosum.
The association of two rare hereditary disorders, trichothiodystrophy (TTD) and xeroderma pigmentosum (XP), was found in four patients from three families, apparently unrelated but living in the same geographical area. In order to test the hypothesis of a common ancestor, consanguinity within and am...
שמור ב:
| הוצא לאור ב: | J Med Genet |
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| Main Authors: | , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMJ Publishing Group
1990
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016874/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2308151/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.1.21 |
| תגים: |
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