CLINICAL MANIFESTATIONS AND CYTOGENETIC OBSERVATIONS OF 7 CASES AFFECTED BY CRI-DU-CHAT SYNDROME

被引：14

作者：

MENNICKEN, U

PFEIFFER, RA

PUYN, U

WORBES, H

WAGENER, A

机构：

来源：

ZEITSCHRIFT FUR KINDERHEILKUNDE | 1968年 / 104卷 / 03期

关键词：

D O I：

10.1007/BF00438902

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：230 / +

页数：1

共 66 条

[51]

Schneegans E, 1966, Pediatrie, V21, P823

[52]

Schroeder H J, 1967, Humangenetik, V4, P294, DOI 10.1007/BF00292202

[53] FINDINGS IN PATIENT WITH APPARENT DELETION OF SHORT ARMS ON ONE OF B GROUP CHROMOSOMES [J].

SIDBURY, JB ;

GRAY, M ;

SCHMICKE.RD .

JOURNAL OF PEDIATRICS, 1964, 65 (6P2) :1098-+

[54]

SILBER DL, 1966, AM J MENT DEF, V71, P486

[55] AUTOSOMAL ABNORMALITIES [J].

SMITH, DW .

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1964, 90 (7P2) :1055-+

[56]

SOLITARE GB, 1967, J MENT DEFIC RES, V11, P267

[57]

STAHL A, 1967, PEDIATRIE, V22, P581

[58] A B-GROUP RING CHROMOSOME WITH MOSAICISM IN A NEWBORN WITH CRI DU CHAT SYNDROME [J].

STEELE, MW ;

BREG, WR ;

EIDELMAN, AI ;

LION, DT ;

TERZAKIS, TA .

CYTOGENETICS, 1966, 5 (06) :419-&

[59]

STUART HC, 1959, TXB PEDIATRICS, P12

[60]

TURNER J. H., 1966, J MED GENET, V3, P66, DOI 10.1136/jmg.3.1.66

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