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

[1] MULTIPLE CONGENITAL ANOMALIES IN A NEGRO INFANT WITH 13-15 TRISOMY
NORTHCUTT, RC
[J]. SOUTHERN MEDICAL JOURNAL, 1962, 55 (04) : 385 - &
[2] MULTIPLE DEVELOPMENTAL ANOMALIES AND TRISOMY OF A 13-15 GROUP CHROMOSOME (D SYNDROME)
CONEN, PE
MAUNTNER, LS
PHILLIPS, KG
[J]. CANADIAN MEDICAL ASSOCIATION JOURNAL, 1962, 87 (13) : 709 - +
[3] NUCLEAR PROJECTIONS OF NEUTROPHILS IN D1 (13-15) TRISOMY SYNDROME
HECHT, F
SCOTT, CR
FINE, RN
WANG, MYF
HEATH, CW
[J]. PEDIATRICS, 1965, 36 (02) : 292 - &
[4] NUCLEAR ABNORMALITIES OF NEUTROPHILS IN D1 (13-15)-TRISOMY SYNDROME
HUEHNS, ER
HECHT, F
LUTZNER, M
[J]. LANCET, 1964, 1 (733): : 589 - &
[5] PROBABLE 3/13-15 CHROMOSOME TRANSLOCATION WITH D1 TRISOMY SYNDROME
ATKINS, L
KEENAN, ME
[J]. JOURNAL OF PEDIATRICS, 1965, 67 (5P1): : 874 - +
[6] NUCLEAR ANOMALIES OF NEUTROPHIL IN A CHROMOSOMAL TRIPLICATION - D1 (13-15) TRISOMY SYNDROME - AN ELECTRON MICROSCOPIC STUDY
LUTZNER, MA
HECHT, F
[J]. LABORATORY INVESTIGATION, 1966, 15 (03) : 597 - &
[7] CONGENITAL DEAFNESS IN 13-15 TRISOMY SYNDROME
MANIGLIA, AJ
WOLFF, D
HERQUES, AJ
[J]. ARCHIVES OF OTOLARYNGOLOGY, 1970, 92 (02): : 181 - &
[8] PICTURE OF MONTH - TRISOMY 13-15 (D TRISOMY - 47,XX OR XY,D1 - PATAUS SYNDROME
GELLIS, SS
FEINGOLD, M
[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1969, 118 (03): : 483 - &
[9] MIDDLE AND INNER EAR ABNORMALITIES - 13-15 (D1) TRISOMY
BLACK, FO
SANDO, I
WAGNER, JA
HEMENWAY, WG
[J]. ARCHIVES OF OTOLARYNGOLOGY, 1971, 93 (06): : 615 - &
[10] PERSISTENCE OF HEMOGLOBIN F IN D/D TRANSLOCATION WITH TRISOMY 13-15 (D1)
PINKERTON, PH
COHEN, MM
[J]. JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1967, 200 (07) : 647 - +

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