CONGENITAL LOCALIZED ABSENCE OF SKIN AND ASSOCIATED ABNORMALITIES RESEMBLING EPIDERMOLYSIS BULLOSA - A NEW SYNDROME

被引：114

作者：

BART, BJ

GORLIN, RJ

ANDERSON, VE

LYNCH, FW

机构：

来源：

关键词：

D O I：

10.1001/archderm.93.3.296

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

引用

页码：296 / &

共 40 条

[1] ABE T, 1964, JAP J DERM, V74, P179
[2] BART BJ, TO BE PUBLISHED
[3] BEATTY W, 1897, BRIT J DERMATOL, V9, P301
[4] CAMPBELL W, 1826, EDINB J MED SCI, V5, P82
[5] Cordon M., 1767, J MED CHIR PHARM, V26, P556
[6] Hereditary epidermolysis bullosa - Report of a case with a resume of the literature
Davidson, LT
[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1940, 59 (02): : 371 - 378
[7] EPSTEIN NN, 1939, ARCH DERM SYPH, V39, P1052
[8] FOX T, 1879, LANCET, V1, P766
[9] FAMILIAL CONGENITAL DEFECT OF THE SCALP
FRANK, L
RUBY, A
[J]. ARCHIVES OF DERMATOLOGY, 1957, 75 (02) : 266 - 267
[10] HEREDITARY SKIN DEFECT IN THE NEWBORN INFANT
FREUD, P
RHODES, AW
WEISZ, A
[J]. JOURNAL OF PEDIATRICS, 1945, 27 (06) : 591 - 594