[Heterosome fragments in gonadal dysgenesis. A contribution on the karyotype--phenotype relationship].

Heterosomenfragmente bei der Gonadendysgenesie. Ein Beitrag zur Bezichung Karyotyp--Phänotyp.

Klinische Wochenschrift ·Vol. 45 ·No. 24 ·1967-12-15 ·Pages 1225-33

Karl HJ, Back F, Macias-Alvarez I, Raith L

Abstract

暂无摘要

MeSH Terms

Adolescent Adult Female Humans Karyotyping Phenotype Sex Chromosome Aberrations Turner Syndrome

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Karl H J

Back F

Macias-Alvarez I

Raith L

References (37)

37 references, click to expand

CLINICAL SIGNIFICANCE OF ANOMALIES OF THE SEX CHROMOSOMES.
Am J Obstet Gynecol. 1965 Oct 1;93:335-42 PMID: 14337371
A probable partial deletion of the Y chromosome in an intersex patient.
Lancet. 1961 Aug 5;2(7197):294-5 PMID: 13695001
Abnormal sexual development associated with sex chromosome mosaicism. Report of three cases.
Pediatrics. 1962 May;29:703-13 PMID: 13892575
[Unilateral renal and bilateral gonadal agenesis with persistent Wolffian duct structures in a case of Turner's syndrome with XO-Xx karyotype].
Ann Endocrinol (Paris). 1965 May-Jun;26(3):291-9 PMID: 5852066
HUMAN SEX CHROMOSOME ABNORMALITIES IN RELATION TO DNA REPLICATION AND HETEROCHROMATINIZATION.
Proc Natl Acad Sci U S A. 1963 May;49(5):581-9 PMID: 16591069
A CASE OF GONADAL DYSGENESIS IN A PATIENT WITH A 46/XY KARYOTYPE, PHALLIC ENLARGEMENT AND ABSENCE OF SEMINIFEROUS TUBULES.
Acta Endocrinol (Copenh). 1964 Nov;47:491-9 PMID: 14225847
[Morphologically abnormal X-chromosomes].
Dtsch Med Wochenschr. 1967 Jan 13;92(2):71-4 PMID: 6016381
An XO/XX/XXX mosaicism in relationship to gonadal dysgenesis in females.
J Clin Endocrinol Metab. 1962 Jul;22:671-7 PMID: 13876802
DNA CONTENT AND AREA OF SEX CHROMATIN IN SUBJECTS WITH STRUCTURAL AND NUMERICAL ABERRATIONS OF THE X CHROMOSOME.
Cytogenetics. 1965;4:96-116 PMID: 14319242
SEX CHROMATIN BODY SIZE AND ITS RELATION TO X CHROMOSOME STRUCTURE.
Cytogenetics. 1965;4:87-95 PMID: 14319241
CLINICAL AND CYTOGENETICAL STUDIES IN FEMALE GONADAL DYSGENESIS AND THEIR BEARING ON THE CAUSE OF TURNER'S SYNDROME.
Cytogenetics. 1964;3:355-83 PMID: 14267131
The chromosomes in a case of pure gonadal dysgenesis.
Br Med J. 1959 Dec 12;2(5162):1285-7 PMID: 14399877
[Turner's syndrome: apropos 6 cases].
Helv Med Acta. 1964 May;31(1):1-28 PMID: 5878387
KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.
J Med Genet. 1965 Jun;2(2):142-55 PMID: 14295659
[ON THE IMMUNOHEMATOLOGIC DETERMINATION OF PITUITARY GONADOTROPINS IN THE URINE].
Klin Wochenschr. 1964 Mar 1;42:246-7 PMID: 14169599
Chromosome preparations of leukocytes cultured from human peripheral blood.
Exp Cell Res. 1960 Sep;20:613-6 PMID: 13772379
[Turner's syndrome with mosaic (XO/X and centromeric fragment)].
Ann Genet. 1965;8(1):50-4 PMID: 5294579
OVARIAN DYSGENESIS DUE TO DELETION OF THE X CHROMOSOME.
Proc Staff Meet Mayo Clin. 1963 Aug 28;38:389-94 PMID: 14047303
Congenital anomalies associated with gonadal aplasia; review of 55 cases.
Pediatrics. 1959 May;23(5):885-902 PMID: 13645125
GONADAL DYSGENESIS WITH AN XY CHROMOSOMAL CONSTITUTION.
Obstet Gynecol. 1964 Nov;24:701-6 PMID: 14227601
[Chromosome anomalies caused by surplus (trisomies) and age of the mother].
Dtsch Med Wochenschr. 1966 Jul 15;91(28):1262-7 PMID: 4223393
AN XY FEMALE WITH ABSENT GONADS AND VESTIGIAL PELVIC ORGANS.
J Obstet Gynaecol Br Commonw. 1963 Aug;70:675-80 PMID: 14078046
A quantitative color reaction for cortisone and related 17,21-dihydroxy-20-ketosteroids.
J Biol Chem. 1950 Jul;185(1):201-7 PMID: 15436491
Haemophilia A in a "girl" with male sex-chromatin pattern.
Lancet. 1959 Sep 5;2(7097):264-6 PMID: 14427266
[Simultaneous determination of cortisol and corticosterone secretory rate in humans].
Z Klin Chem Klin Biochem. 1968 Jun;6(4):346-9 PMID: 4882484
The drumsticks of polymorphonuclear leucocytes in sex-chromosome abnormalities.
Lancet. 1962 Jun 2;1(7240):1154-8 PMID: 14468013
[Deviations in the sex chromosome findings of a rare special form of intersexuality with missing internal genital organs].
Cytogenetics. 1965;4(6):349-64 PMID: 5893750
GONADAL DYSGENESIS: A REVIEW AND REPORT OF A CASE WITH AN UNUSUAL CHROMOSOMAL ABERRATION.
Lahey Clin Found Bull. 1964 Apr-Jun;13:181-9 PMID: 14171917
[On the Turner syndrome. On the personality analysis of child and adult Turner patients].
Dtsch Med Wochenschr. 1967 Mar 10;92(10):417-22 PMID: 6019585
CYTOGENETIC AND CLINICAL FINDINGS IN 48 PATIENTS WITH CONGENITALLY DEFECTIVE OR ABSENT OVARIES.
Medicine (Baltimore). 1965 Mar;44:135-64 PMID: 14272749
Sex chromatin and gene action in the mammalian X-chromosome.
Am J Hum Genet. 1962 Jun;14:135-48 PMID: 14467629
Abnormalities involving the X chromosome in women.
Lancet. 1960 Jun 4;1(7136):1213-6 PMID: 14406379
Cytogenetical and clinical observations in female gonadal dysgenesis.
Acta Endocrinol Suppl (Copenh). 1962;40(Suppl 65):1-122 PMID: 13878157
TWO XY SIBLINGS WITH GONADAL DYSGENESIS AND A FEMALE PHENOTYPE.
N Engl J Med. 1965 May 27;272:1083-8 PMID: 14281549
GONADAL DYSGENESIS DUE TO MOSAICISM OF AN X CHROMOSOME FRAGMENT.
Proc Staff Meet Mayo Clin. 1963 Sep 11;38:422-6 PMID: 14064415
Deletion of Y chromosome in a family with muscular dystrophy and hypospadias.
Br Med J. 1962 Feb 3;1(5274):291-4 PMID: 14477078
[A case of pure gonadal agenesis of female phenotype and XY karyotype].
Ann Endocrinol (Paris). 1965 Sep-Oct;26(5):572-82 PMID: 5853811

Article Info

Journal

Klinische Wochenschrift

Abbr.

Klin Wochenschr

ISSN

0023-2173

DOI

10.1007/BF01746268

Published

1967-12-15

Pages

1225-33

Language

ger

Region

Germany

NLM ID

2985205R

Subset

External Links

PubMed source DOI: 10.1007/BF01746268

Analysis Services

[Heterosome fragments in gonadal dysgenesis. A contribution on the karyotype--phenotype relationship].

Contact

WeChat Official Account