Steinbach P, Horstmann W, Scholz W
Hum Genet. 1980; 54(3):309-13.
PMID: 7399525
DOI: 10.1007/BF00291574.
THERMAN E, Denniston C, Sarto G, Ulber M
Hum Genet. 1980; 54(2):133-43.
PMID: 7390488
DOI: 10.1007/BF00278961.
Mattei M, Mattei J, Ayme S, Giraud F
Hum Genet. 1982; 61(4):295-309.
PMID: 7152515
DOI: 10.1007/BF00276593.
Duckett D, Roberts S
Hum Genet. 1981; 58(4):377-86.
PMID: 7035334
DOI: 10.1007/BF00282819.
Camargo M, cervenka J
Hum Genet. 1984; 67(1):37-47.
PMID: 6745924
DOI: 10.1007/BF00270556.
Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.
Mattei M, Souiah N, Mattei J
Hum Genet. 1984; 66(4):313-34.
PMID: 6373566
DOI: 10.1007/BF00287636.
Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.
Duckett D, Roberts S, Davies P
Hum Genet. 1984; 67(2):156-61.
PMID: 6336319
DOI: 10.1007/BF00272991.
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.
[Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)].
DOLLMANN A, NOCKE W, Stengel-Rutkowski S
Humangenetik. 1972; 14(4):285-99.
PMID: 5051752
DOI: 10.1007/BF00290170.
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.
Apparently isodicentric but functionally monocentric X chromosome in man.
THERMAN E, Sarto G, PATAU K
Am J Hum Genet. 1974; 26(1):83-92.
PMID: 4130093
PMC: 1762552.
Investigation of the "variable spreading" of X inactivation into a translocated autosome.
Schanz S, Steinbach P
Hum Genet. 1989; 82(3):244-8.
PMID: 2731936
DOI: 10.1007/BF00291163.
Aspermia, associated with a presumably balanced X/autosomal translocation karyotype 46, Y, t (X;5) (q28;q11).
Stengel-Rutkowski S, Zankl H, Rodewald A, Scharrer S, CHAUDHURI J, Zang K
Hum Genet. 1976; 31(1):97-106.
PMID: 1248827
DOI: 10.1007/BF00270405.
Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation.
LEISTI J, Kaback M, Rimoin D
Am J Hum Genet. 1975; 27(4):441-53.
PMID: 1155455
PMC: 1762798.
A dynamic study in two new cases of X chromosome translocations.
Mattei M, Mattei J, Ayme S, Malpuech G, Giraud F
Hum Genet. 1978; 41(3):251-7.
PMID: 649152
DOI: 10.1007/BF00284758.
X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.
Bernstein R, Dawson B, Kohl R, Jenkins T
J Med Genet. 1979; 16(4):254-62.
PMID: 290816
PMC: 1012665.
DOI: 10.1136/jmg.16.4.254.
Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21).
Couturier J, Dutrillaux B, Garber P, Raoul O, Croquette M, FOURLINNIE J
Hum Genet. 1979; 49(3):319-26.
PMID: 157971
DOI: 10.1007/BF00569351.
[Four new cases of X-autosome translocation in man (author's transl)].
Laurent C, Biemont M, Dutrillaux B
Humangenetik. 1975; 26(1):35-46.
PMID: 50265
DOI: 10.1007/BF00280283.
