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[Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)].
Ann Genet. 1970 Dec;13(4):245-8
PMID: 5313888
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[46, XXip karyotype in a woman with normal stature and gonadal dysgenesis without other congenital anomalies].
Humangenetik. 1973;20(2):163-6
PMID: 4785163
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A CASE OF PRIMARY AMENORRHEA WITH A TRANSLOCATION INVOLVING CHROMOSOMES OF GROUPS B AND C.
Am J Hum Genet. 1965 Sep;17:377-83
PMID: 14334736
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Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers).
Proc Natl Acad Sci U S A. 1972 Jan;69(1):69-73
PMID: 4500556
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Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.
Am J Hum Genet. 1971 Jul;23(4):410-8
PMID: 5097907
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Two human X-autosome translocations identified by autoradiography and fluorescence.
Am J Hum Genet. 1972 Sep;24(5):583-97
PMID: 5054227
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Increased Q fluorescence of an inactive Xq-chromosome in man.
Clin Genet. 1974;6(4):289-93
PMID: 4442233
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Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.
J Med Genet. 1971 Sep;8(3):358-63
PMID: 5097143
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Trisomy 13 with a 13-X translocation.
Am J Hum Genet. 1974 May;26(3):385-92
PMID: 4133276
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Human genetics.
Annu Rev Genet. 1973;7:435-72
PMID: 4131531
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Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes.
Proc Natl Acad Sci U S A. 1973 Dec;70(12):3395-9
PMID: 4128545
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X inactivation in man: a woman with t(Xq--;12q+).
Am J Hum Genet. 1973 May;25(3):262-70
PMID: 4704858
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Cytogenetic and clinical study on 100 cases of primary amenorrhoea.
Acta Obstet Gynecol Scand Suppl. 1973;:1-78
PMID: 4518464
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X-autosome translocation in normal mother and effectively 21-monosomic daughter.
J Pediatr. 1974 Apr;84(4):539-46
PMID: 4834247
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Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
Cytogenet Cell Genet. 1973;12(5):357-66
PMID: 4131091
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Evidence for X-X chromosome translocation in humans.
Ann Hum Genet. 1969 Oct;33(2):117-24
PMID: 5383978
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Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome.
J Med Genet. 1970 Mar;7(1):1-4
PMID: 5480961
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Non-random late replication of X chromosomes in mules and hinnies.
Nature. 1971 Jul 30;232(5309):315-9
PMID: 5094835
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An inherited X-autosome translocation in man.
Ann Hum Genet. 1971 Oct;35(2):171-8
PMID: 5159532
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Center for Barr body condensation on the proximal part of the human Xq: a hypothesis.
Chromosoma. 1974 Jan 29;44(4):361-6
PMID: 4134866
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Apparently isodicentric but functionally monocentric X chromosome in man.
Am J Hum Genet. 1974 Jan;26(1):83-92
PMID: 4130093
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Banding patterns and autoradiographic studies of cells with an X-autosome translocation.
Ann Hum Genet. 1973 Jul;37(1):9-12
PMID: 4128188
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[Turner syndrome 45,X-46,XXq+].
Ann Endocrinol (Paris). 1970 Nov-Dec;31(6):1153-5
PMID: 5509948
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Gonadal Dysgenesis with Unusual Abnormalities.
Arch Dis Child. 1965 Jun;40(211):274-9
PMID: 21032420
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Fluorescence and Giemsa banding studies of the allocyclic X chromosome in embryonic and adult mouse cells.
Exp Cell Res. 1973 Mar 30;78(1):127-35
PMID: 4120564
-
Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis.
Ann Hum Genet. 1967 May;30(4):313-23
PMID: 5619932
-
X-autosome translocations in the mouse: total inactivation versus partial inactivation of the X chromosome.
Adv Genet. 1970;15:175-259
PMID: 4936423
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A marker X chromosome.
Am J Hum Genet. 1969 May;21(3):231-44
PMID: 5794013
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[Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+].
Cytogenetics. 1971;10(2):87-98
PMID: 5098032
-
Presumptive x-autosome translocation in a cow: preferential inactivation of the normal x chromosome.
Nature. 1968 Apr 13;218(5137):183-4
PMID: 5645293
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Inactivation of the x-chromosome.
N Engl J Med. 1972 Feb 10;286(6):318-9
PMID: 5061691
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The single-active-X: functional differentiation at the chromosome level.
Natl Cancer Inst Monogr. 1967 Sep;26:327-51
PMID: 4864109
-
The nature of structural X chromosome aberrations in Turner's syndrome as revealed by quinacrine mustard fluorescence analysis.
Hereditas. 1970;66(2):287-92
PMID: 5525826
-
[Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)].
Humangenetik. 1972;14(4):285-99
PMID: 5051752
-
THE LYON-BEUTLER HYPOTHESIS AND ISOCHROMOSOME X PATIENTS WITH TURNER SYNDROME.
Lancet. 1963 Aug 24;2(7304):411
PMID: 14044304
-
Cytogenetics of fifty patients with primary amenorrhea.
Am J Obstet Gynecol. 1974 May 1;119(1):14-23
PMID: 4820908
-
Anomalies of development in a girl with unusual sex chromosomal mosaicism.
J Med Genet. 1967 Dec;4(4):283-7
PMID: 6082908
-
Autoradiographic investigations of centric fragments and rings in patients with stigmata of gonadal dysgenesis.
Cytogenetics. 1967;6(3):254-67
PMID: 6040474
-
A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME.
Cytogenetics. 1964;3:427-40
PMID: 14267135
-
Genetic activity of sex chromosomes in somatic cells of mammals.
Philos Trans R Soc Lond B Biol Sci. 1970 Aug 6;259(828):41-52
PMID: 4399067
-
An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.
Clin Genet. 1972;3(5):388-95
PMID: 4117330
-
Possible X-autosomal translocation in a girl with gonadal dysgenesis.
J Med Genet. 1970 Dec;7(4):402-6
PMID: 5501708
-
Isochromosome for the short arm of X, a human 46, XXpi syndrome.
Ann Hum Genet. 1972 Jul;36(1):79-87
PMID: 4656769
-
[X-CHROMOSOME ANOMALY AND AHAPTOGLOBINEMIA IN HEMOPHILIA A].
Acta Haematol. 1965 Jan;33:49-56
PMID: 14286001
-
X-chromosome inactivation and the Xg locus.
Am J Hum Genet. 1970 Jul;22(4):460-3
PMID: 5432290
-
[Ring chromosomes and centric fragments in Turner's syndrome].
Geburtshilfe Frauenheilkd. 1968 Jan;28(1):11-26
PMID: 5668618