CASE OF LONG ARM DELETION OF THE X-CHROMOSOME IN A PATIENT WITH SECONDARY AMENORRHEA

被引：16

作者：

BRANKOVIC, S ^{[1
]}

LACA, Z ^{[1
]}

DRAMUSIC, V ^{[1
]}

IVANOVIC, M ^{[1
]}

MORICPETROVIC, S ^{[1
]}

机构：

[1] INST MOTHER & CHILD PROTECT, BELGRADE, YUGOSLAVIA

来源：

HUMAN GENETICS | 1979年 / 48卷 / 01期

关键词：

D O I：

10.1007/BF00273289

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

This paper presents the clinical and cytogenetic findings in a female patient with secondary amenorrhea and normal phenotype. Some difficulties related to karyotype-phenotype correlation are discussed. © 1979 Springer-Verlag.

引用

页码：139 / 142

页数：4

共 7 条

[1] SOMATIC STIGMATA OF TURNERS SYNDROME IN A PATIENT WITH 46,XXQ-
BOCIAN, M
KRMPOTIC, E
SZEGO, K
ROSENTHAL, IM
[J]. JOURNAL OF MEDICAL GENETICS, 1971, 8 (03) : 358 - +
[2] FLUORESCENCE AND AUTORADIOGRAPHIC STUDIES IN PATIENTS WITH TURNERS SYNDROME AND 46,XXP- AND 46,XXQ- KARYOTYPES
BOCZKOWSKI, K
MIKKELSEN, M
[J]. JOURNAL OF MEDICAL GENETICS, 1973, 10 (04) : 350 - 355
[3] CHAPELLE ADL, 1975, HEREDITAS, V80, P113
[4] DUTRILLAUX B, 1973, CR ACAD SCI D NAT, V276, P3179
[5] FORABOSC.A, 1974, LANCET, V2, P403
[6] HECHT F, 1970, Journal of Medical Genetics, V7, P1, DOI 10.1136/jmg.7.1.1
[7] SEABRIGH.M, 1971, LANCET, V2, P971

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