SCOPUS 정보 검색 플랫폼

Volumn 98, Issue 3, 2001, Pages 269-272

New syndrome? Proximal symphalangism with "coarse" facial appearance, mixed hearing loss, and chronic renal failure: New malformation syndrome?

(8) Morimoto, Junko a Kaneoka, Hidetoshi b Murata, Toshiaki c Sato, Yumi Nakai c Ogahara, Satoru c Hirose, Shinichi c Naito, Setsuya c Naritomi, Kenji c

a FUKUOKA UNIVERSITY HOSPITAL (Japan)

b FUKUOKA UNIVERSITY (Japan)

c UNIVERSITY OF THE RYUKYUS SCHOOL OF MEDICINE (Japan)

Author keywords

Endstage renal disease; Malformation syndrome; Mixed hearing loss; Proximal symphalangism

Indexed keywords

ADULT; ARTICLE; BIRTH WEIGHT; CASE REPORT; CHRONIC KIDNEY FAILURE; EDEMA; FACE MALFORMATION; FINGER MALFORMATION; HEARING LOSS; HEMODIALYSIS; HUMAN; HUMAN TISSUE; KIDNEY BIOPSY; MALE; MALFORMATION SYNDROME; MENTAL DEFICIENCY; PERITONEAL DIALYSIS; PRIORITY JOURNAL; PROTEINURIA; SHORT STATURE; SKELETON MALFORMATION; SYNDROME DELINEATION; CONGENITAL MALFORMATION; FACE; FINGER JOINT; HEARING DISORDER; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; SYNDROME;

VALGUS;

ABNORMALITIES, MULTIPLE; ADULT; FACE; FINGER JOINT; HEARING DISORDERS; HUMANS; KIDNEY FAILURE, CHRONIC; MALE; SYNDROME;

EID: 0035931460 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/1096-8628(20010122)98:3<269::AID-AJMG1079>3.0.CO;2-1 Document Type: Article

Times cited : (4)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.