AUTOPSY CASE OF D1 (13-15) TRISOMY SYNDROME WITH MULTIPLE CONGENITAL ANOMALIES

被引：0

作者：

KIHARA, M ^{[1
]}

KAWAI, K ^{[1
]}

SHIMODA, H ^{[1
]}

机构：

[1] NAGASAKI UNIV,SCH MED,DEPT SURG,NAGASAKI 852,JAPAN

来源：

ACTA PATHOLOGICA JAPONICA | 1979年 / 29卷 / 06期

关键词：

D O I：

暂无

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

引用

页码：1013 / 1022

页数：10

共 50 条

[21] AUTODARIOGRAPHIC IDENTIFICATION OF D(13-15) CHROMOSOME RESPONSIBLE FOR D1 TRISOMIC PATAUS SYNDROME
GIANNELLI, F
[J]. NATURE, 1965, 208 (5011) : 669 - +
[22] FEATURES OF 13-15 TRISOMY SYNDROME WITH NORMAL KARYOTYPE
MARSHALL, R
ELLIS, JR
NEWNHAM, RE
STEVENS, LJ
RAWSTRON, JR
[J]. LANCET, 1964, 1 (733): : 556 - &
[23] A SPECIFIC CONGENITAL DEFECT OF BRAIN ASSOCIATED WITH 13-15 TRISOMY
MILLER, JQ
PICARD, E
GERALD, PS
ALKAN, M
WARNER, S
[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1962, 104 (05): : 532 - &
[24] STUDIES ON DEVELOPMENT OF EYE IN 13-15 TRISOMY SYNDROME
ROCH, LM
PETRUCCI, JV
BARBER, AN
[J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1965, 60 (06) : 1067 - &
[25] IMMUNOGLOBULINS IN 13-15 TRISOMY SYNDROME DUE TO A TRANSLOCATION
GUSTAVSON, KH
JOHANSSON, SG
WRANNE, L
[J]. ACTA PAEDIATRICA SCANDINAVICA, 1968, 57 (05): : 436 - +
[26] A SPECIFIC CONGENITAL BRAIN DEFECT (ARHINENCEPHALY) IN 13-15 TRISOMY
MILLER, JQ
ALKAN, MK
GERALD, PS
PICARD, EH
WARNER, S
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1963, 268 (03): : 120 - &
[27] CASE OF D1 TRISOMY SYNDROME SHOWING MULTIPLE TISSUE MALFORMATIONS
FURUTA, M
TAKEUCHI, T
ASAMOTO, H
[J]. TERATOLOGY, 1972, 6 (01) : 106 - &
[28] PERSISTENCE OF STAPEDIAL ARTERY IN TRISOMY 13-15 SYNDROME
SANDO, I
HEMENWAY, WG
BLACK, FO
BAKER, B
[J]. ARCHIVES OF OTOLARYNGOLOGY, 1972, 96 (05): : 441 - &
[29] CASE OF TRISOMY D1 - SYNDROME OF PATAU
GUANTI, G
DELSORDO, F
PETRINELLI, P
BATTAGLIA, E
[J]. CARYOLOGIA, 1970, 23 (04) : 489 - +
[30] OCULAR ANOMALIES IN TRISOMY 13-15 - ANALYSIS OF 13 EYES WITH 2 NEW FINDINGS
HOEPNER, J
YANOFF, M
[J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1972, 74 (04) : 729 - &

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