共 15 条
- [1] SPORADIC CASE OF APPARENT APROSENCEPHALY [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 3 (03): : 311 - 314
- [2] PRELIMINARY DEFINITION OF A CRITICAL REGION OF CHROMOSOME-13 IN Q32 - REPORT OF 14 CASES WITH 13Q DELETIONS AND REVIEW OF THE LITERATURE [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 45 (01): : 52 - 59
- [4] GARCIA CA, 1977, DEV MED CHILD NEUROL, V19, P227
- [5] MOSAIC R(13) IN AN INFANT WITH APROSENCEPHALY [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (04): : 531 - 533
- [7] LIVANAINEN M, 1977, DEV MED CHILD NEUROL, V19, P663
- [8] APROSENCEPHALY-ATELENCEPHALY AND THE APROSENCEPHALY (XK) SYNDROME [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 3 (03): : 303 - 309
- [9] THE XK-APROSENCEPHALY SYNDROME [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 7 (02): : 231 - 234
- [10] A REVIEW AND CASE-REPORT OF APROSENCEPHALY AND THE XK APROSENCEPHALY SYNDROME [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 11 (03): : 369 - 371