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Abnormalities of human sex chromosomes. II. Turner's syndrome associated with the mosaicism 45,X-46, XX-p.
Ann Genet. 1971 Jun;14(2):105-11
PMID: 5314796
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[Familial X-autosomal translocation t (X, 2)].
Tsitologiia. 1976 Jul;18(7):901-5
PMID: 982591
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Deletion mapping of the human X chromosome.
Hereditas. 1975;80(1):113-20
PMID: 1141012
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Dicentric X isochromosomes in man.
J Med Genet. 1976 Dec;13(6):496-500
PMID: 1018308
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X-inactivation pattern in three cases of X/autosome translocation.
Am J Med Genet. 1978;1(3):309-17
PMID: 677170
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Isodicentric X chromosome in a woman with characteristics of gonadal dysgenesis.
Hum Genet. 1979 Jun 19;49(2):237-41
PMID: 468255
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X short arm deletion in a female subject with spontaneous sexual development.
Am J Obstet Gynecol. 1979 Feb 15;133(4):460-1
PMID: 434013
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Short-arm deletion of an X chromosome (45,XO/46,XX p--).
Hum Genet. 1977 Jun 10;37(1):93-6
PMID: 881199
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Presumptive evidence of two active X chromosomes in somatic cells of a human female.
Nature. 1977 Jan 13;265(5590):142-4
PMID: 834254
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[Identification of a dicentric isochromosome (X dic qi) in a case of gonadal dysgenesis].
Pediatrie. 1977 Jun;32(4):383-8
PMID: 887359
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Reduced phenotypic effect on partial trisomy 1q in a X/1 translocation.
Ann Genet. 1977 Sep;20(3):191-94
PMID: 304704
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Position of the human X inactivation center on Xq.
Hum Genet. 1979;50(1):59-64
PMID: 468261
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A case of partial trisomy 17 resulting from X-autosomal translocation.
J Med Genet. 1979 Oct;16(5):395-9
PMID: 513087
-
[Morphologically abnormal X-chromosomes].
Dtsch Med Wochenschr. 1967 Jan 13;92(2):71-4
PMID: 6016381
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Dicentric human X chromosomes.
Hereditas. 1974;76(2):259-68
PMID: 4135824
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X-X translocation in a patient with gonadal dysgenesis and the problems of phenotype-karyotype correlations.
Hum Genet. 1978 Feb 16;40(3):249-57
PMID: 631846
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Spreading of inactivation in an (X;14) translocation.
Am J Med Genet. 1978;2(3):233-40
PMID: 263441
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Cytogenetic studies in seven individuals with an i(Xq) karyotype.
Hereditas. 1977;86(1):121-8
PMID: 903248
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[A second example of telomeric fusion 2 X chromosomes].
Ann Genet. 1975 Dec;18(4):243-5
PMID: 1083194
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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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Chromosome studies in 30 children with Turner's syndrome.
Acta Paediatr Scand. 1972 Jan;61(1):17-23
PMID: 5018573
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A dynamic study in two new cases of X chromosome translocations.
Hum Genet. 1978 Apr 24;41(3):251-7
PMID: 649152
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Structural aberrations of the X chromosome in man.
Hum Genet. 1978 Apr 24;41(3):269-79
PMID: 649155
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Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism.
J Med Genet. 1978 Jun;15(3):222-6
PMID: 671488
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Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter).
Hum Genet. 1977 Nov 10;39(2):147-55
PMID: 598825
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Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 [inv(2) (p15 q21)] in a patient with gonadal dysgenesis.
Clin Genet. 1975 Jul;8(1):11-7
PMID: 1149316
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Follow-up on a human X-autosome translocation first studied in 1963 and 1964.
Birth Defects Orig Artic Ser. 1978;14(6C):365-75
PMID: 728592
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Short arm deletion of an X chromosome, 46,XXp-.
Hum Genet. 1976 Apr 15;32(1):89-100
PMID: 1262028
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A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea.
Hum Genet. 1979 Apr 17;48(1):139-42
PMID: 457130
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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
-
Differences in human X isochromosomes.
J Med Genet. 1975 Dec;12(4):378-89
PMID: 1219118
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Isochromosome X in man: different DNA replication patterns in the long arms.
Hum Genet. 1976 Jul 7;33(1):55-60
PMID: 939557
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Cytogenetic studies in primary amenorrhoea.
Lancet. 1961 Jun 3;1(7188):1183-9
PMID: 13718574
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Gonadal dysgenesis in phenotypic female subjects. A review of eighty-seven cases, with cytogenetic studies in fifty-three.
Am J Med. 1968 Oct;45(4):529-43
PMID: 5678097
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Isochromosome for the short arm of X with primary amenorrhoea and a pituitary tumour.
Aust N Z J Med. 1973 Dec;3(6):617-9
PMID: 4522699
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X-short arm deletion gonadal dysgenesis in two siblings due to unique translocation (Xp-;16p+).
Clin Genet. 1976 Oct;10(4):202-7
PMID: 975595
-
X-autosome translocation in normal mother and effectively 21-monosomic daughter.
J Pediatr. 1974 Apr;84(4):539-46
PMID: 4834247
-
[X chromosome with deletion of the long arm].
J Gynecol Obstet Biol Reprod (Paris). 1977 Apr-May;6(3):337-45
PMID: 903575
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An inherited X-autosome translocation in man.
Ann Hum Genet. 1971 Oct;35(2):171-8
PMID: 5159532
-
Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq).
Clin Genet. 1975 Apr;7(4):299-303
PMID: 47795
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Letter: X long-arm deletion with features of Turner's syndrome.
Lancet. 1974 Aug 17;2(7877):403-4
PMID: 4137037
-
Isochromosome for the short arm of X: a human mosaic 45,x/46,XXpi.
Clin Genet. 1975 Feb;7(2):148-54
PMID: 1132163
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Fusion of the short arms of one X chromosome in a patient with gonadal dysgenesis.
Humangenetik. 1974;24(2):159-60
PMID: 4430496
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Letter: A case of primary amenorrhea associated with X-autosomal translocation (46,X,t(Xq minus;5q plus)).
Am J Hum Genet. 1974 May;26(3):416
PMID: 4827371
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Apparent deletion of X chromosome in a prepuberal girl.
J Med Genet. 1966 Sep;3(3):226-9
PMID: 5971058
-
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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A case of 46,X,t(X;X)(pter to q27::q27 to pter)/47,X,t(X;X) (pter to q27::q27 to pter), + mar/48,XX,t(X;X)(pter to q27::q27 to pter), + mar and a functionally monocentric translocation X.
Ann Genet. 1977 Jun;20(2):119-21
PMID: 302685
-
Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation.
Am J Hum Genet. 1975 Jul;27(4):441-53
PMID: 1155455
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Replication pattern of the X chromosomes in three X/autosomal translocations.
Cytogenet Cell Genet. 1977;18(6):333-48
PMID: 884969
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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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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
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BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.
Chromosoma. 1976 Aug 17;57(2):135-53
PMID: 954550
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A girl with mosaicism for a dicentric X chromosome (45,X/46,X,dic(X) (Xqter to p22::p22 to qter)).
Hum Genet. 1977 Aug 31;38(1):39-48
PMID: 903154
-
Turner syndrome with rare karyotypes.
Clin Genet. 1978 May;13(5):409-14
PMID: 657581
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Center for Barr body condensation. A case of Turner's syndrome with 45,X/46,X,dic(X) (Xqter leads to p22::p22 leads to qter).
Hum Genet. 1976 Aug 30;33(3):337-40
PMID: 964996
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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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Fluorescence and autoradiographic studies in patients with Turner's syndrome and 46,XXp- and 46,XXq- karyotypes.
J Med Genet. 1973 Dec;10(4):350-5
PMID: 4129970
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Chromosomal and clinical findings in 110 females with Turner syndrome.
Hum Genet. 1976 Dec 29;35(1):35-49
PMID: 1002163
-
Genetic and clinical considerations of long-arm deletion of the X chromosome.
Pediatrics. 1970 Apr;45(4):656-64
PMID: 5438168
-
Reappraisal of a 46,X,i(Xp) karyotype as 46,X,del(Xg).
Hereditas. 1975;80(1):137-40
PMID: 1141014
-
Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertile.
Hum Genet. 1977 Dec 23;39(3):283-92
PMID: 598836
-
Gonadal dysgenesis with lymphocytic thyroiditis and deletion of the long arm of the X chromosome.
Acta Paediatr Scand. 1969 Nov;58(6):625-31
PMID: 5395875
-
Fusion of two apparently intact human X chromosomes.
Hum Genet. 1976 Jun 29;32(3):295-300
PMID: 939549