| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0022-3476(05)82547-8 |
| P698 | PubMed publication ID | 1385628 |
| P2093 | author name string | K Tsuji | |
| Y Seino | |||
| Y Yokoyama | |||
| K Narahara | |||
| M Kamada | |||
| P2860 | cites work | Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito. | Q34645820 |
| Mosaic trisomy 16 in a live newborn infant | Q38364955 | ||
| Further observations of cell selection in vivo in normal-G trisomic mosaics | Q44122881 | ||
| Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis. | Q52249239 | ||
| Pre- and postnatal diagnosis of trisomy 4 mosaicism | Q68635174 | ||
| Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study | Q69292175 | ||
| Confined chorionic mosaicism in prenatal diagnosis | Q69398560 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | congenital heart disease | Q939364 |
| P304 | page(s) | 80-82 | |
| P577 | publication date | 1992-07-01 | |
| P1433 | published in | The Journal of Pediatrics | Q7743611 |
| P1476 | title | Tissue-specific mosaicism for trisomy 21 and congenital heart disease | |
| P478 | volume | 121 |
| Q40749209 | A second case of intrauterine growth retardation and primary hypospadias associated with a trisomy 22 placenta but with biparental inheritance of chromosome 22 in the fetus |
| Q70579909 | Congenital heart disease in trisomy 21 mosaicism |
| Q38737280 | Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations |
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