טוען...
Trisomy 10p syndrome owing to maternal pericentric inversion.
A female infant with karyotype 46,XX,rec(10),dup p inv(10)(p11.2q25.2)mat is presented. She had both duplication of 10p and deletion of distal 10q, but only had the constellation of specific features characteristic of duplication of 10p. IMAGES:
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/PMC1017032/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2182876/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.4.264 |
| תגים: |
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