Du H, Sun Y, Zhang Y, Wang S, Zhu H, Chen S
Front Endocrinol (Lausanne). 2022; 13:963827.
PMID: 35957820
PMC: 9360486.
DOI: 10.3389/fendo.2022.963827.
Lee S, Lee S, Chung T, Kim H, Yoon T, Kwak I
J Assist Reprod Genet. 2003; 20(9):385-9.
PMID: 14531651
PMC: 3455837.
DOI: 10.1023/a:1025437329427.
Ogata T, Matsuo N
Hum Genet. 1993; 91(6):551-62.
PMID: 8340109
DOI: 10.1007/BF00205079.
Ogata T, Matsuo N
Hum Genet. 1995; 95(6):607-29.
PMID: 7789944
DOI: 10.1007/BF00209476.
Carpenter N, Say B, Browning D
J Med Genet. 1980; 17(3):216-21.
PMID: 7401133
PMC: 1048550.
DOI: 10.1136/jmg.17.3.216.
Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation.
Steinbach P, Horstmann W, Scholz W
Hum Genet. 1980; 54(3):309-13.
PMID: 7399525
DOI: 10.1007/BF00291574.
X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter.
Madan K, Hompes P, Schoemaker J, Ford C
Hum Genet. 1981; 59(4):290-6.
PMID: 7333583
DOI: 10.1007/BF00295460.
Structural anomalies of the X chromosome and inactivation center.
Mattei M, Mattei J, Vidal I, Giraud F
Hum Genet. 1981; 56(3):401-8.
PMID: 7239523
DOI: 10.1007/BF00274702.
Clinical consequences of Xp-.
Egozcue J
Hum Genet. 1980; 55(1):141-2.
PMID: 7192687
DOI: 10.1007/BF00329143.
X-autosome translocations: cytogenetic characteristics and their consequences.
Mattei M, Mattei J, Ayme S, Giraud F
Hum Genet. 1982; 61(4):295-309.
PMID: 7152515
DOI: 10.1007/BF00276593.
Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly.
FAED M, Lamont M, Baxby K
J Med Genet. 1982; 19(1):49-56.
PMID: 7069747
PMC: 1048819.
DOI: 10.1136/jmg.19.1.49.
Inactivation centers in the human X chromosome.
NAKAGOME Y
Am J Hum Genet. 1982; 34(2):182-94.
PMID: 6985472
PMC: 1685292.
Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse.
MIGEON B, Brown T, Axelman J, Migeon C
Proc Natl Acad Sci U S A. 1981; 78(10):6339-43.
PMID: 6947233
PMC: 349034.
DOI: 10.1073/pnas.78.10.6339.
Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocation.
COHEN M, Charrow J, Balkin N, Harris C
Am J Hum Genet. 1983; 35(4):635-44.
PMID: 6881140
PMC: 1685733.
Highly polymorphic DNA site D14S1 maps to the region of Burkitt lymphoma translocation and is closely linked to the heavy chain gamma 1 immunoglobulin locus.
Balazs I, Purrello M, Rubinstein P, Alhadeff B, SINISCALCO M
Proc Natl Acad Sci U S A. 1982; 79(23):7395-9.
PMID: 6818543
PMC: 347346.
DOI: 10.1073/pnas.79.23.7395.
DNA replication and inactivation patterns in structural abnormality of sex chromosomes. I.X-A translocations, rings, fragments, isochromosomes, and pseudo-isodicentrics.
Camargo M, cervenka J
Hum Genet. 1984; 67(1):37-47.
PMID: 6745924
DOI: 10.1007/BF00270556.
Balanced structural changes involving the human X: effect on sexual phenotype.
Madan K
Hum Genet. 1983; 63(3):216-21.
PMID: 6343223
DOI: 10.1007/BF00284652.
Two human X-autosome translocations identified by autoradiography and fluorescence.
COHEN M, Lin C, Sybert V, Orecchio E
Am J Hum Genet. 1972; 24(5):583-97.
PMID: 5054227
PMC: 1762175.
X inactivation in man: a woman with t(Xq--;12q+).
Sarto G, THERMAN E, PATAU K
Am J Hum Genet. 1973; 25(3):262-70.
PMID: 4704858
PMC: 1762535.
Abnormal X chromosomes in man: origin, behavior and effects.
THERMAN E, PATAU K
Humangenetik. 1974; 25(1):1-16.
PMID: 4475024
DOI: 10.1007/BF00281002.
