共 16 条
- [1] PROBABLE AUTOSOMAL RECESSIVE INHERITANCE OF POLYSPLENIA, SITUS INVERSUS AND CARDIAC DEFECTS IN AN AMISH FAMILY [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 16 (01): : 35 - 42
- [3] MONOSOMY OF CHROMOSOME NO 22 - CASE REPORT [J]. JOURNAL OF PEDIATRICS, 1973, 83 (05) : 836 - 838
- [5] FERENCZ C, 1990, DEVELOPMENTAL CARDIOLOGY, P523
- [6] HURWITZ RC, 1982, CLIN GENET, V22, P7
- [7] KATCHER AL, 1980, PEDIATRICS, V65, P633
- [8] X-LINKED LATERALITY SEQUENCE - SITUS-INVERSUS, COMPLEX CARDIAC DEFECTS, SPLENIC DEFECTS [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (01): : 111 - 116
- [9] AGNATHIA, HOLOPROSENCEPHALY, AND SITUS-INVERSUS - A 3RD REPORT [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 37 (02): : 286 - 287
- [10] FAMILIAL CLUSTERING OF SITUS INVERSUS TOTALIS, AND ASPLENIA AND POLYSPLENIA SYNDROMES [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 16 (01): : 43 - 47