Graves J
Bioessays. 2016; 38(8):734-43.
PMID: 27334831
PMC: 5094562.
DOI: 10.1002/bies.201600019.
Mozdarani H, Meybodi A, Zari-Moradi S
Indian J Hum Genet. 2010; 14(1):1-6.
PMID: 20300283
PMC: 2840781.
DOI: 10.4103/0971-6866.42319.
Micic M, Nikolis J, Micic S
Hum Genet. 1980; 55(1):137-9.
PMID: 7450751
DOI: 10.1007/BF00329142.
Navarro J, Vidal F, Guitart M, Egozcue J
Hum Genet. 1981; 59(4):419-21.
PMID: 7333595
DOI: 10.1007/BF00295483.
Egozcue J, Marina S, Templado C
J Med Genet. 1981; 18(5):362-5.
PMID: 7328616
PMC: 1048758.
DOI: 10.1136/jmg.18.5.362.
Pericentric inversion of chromosome 1 in three sterile brothers.
Giraldo A, Silva E, Martinez I, Campos C, Guzman J
Hum Genet. 1981; 58(2):226-7.
PMID: 7287009
DOI: 10.1007/BF00278718.
Meiotic findings in human reciprocal 1;3 translocation.
Micic M, Micic S
Hum Genet. 1981; 57(4):442-3.
PMID: 7286989
DOI: 10.1007/BF00281703.
Clinical manifestations of familial 13;18 translocation.
Blattner W, Kistenmacher M, Tsai S, Punnett H, GIBLETT E
J Med Genet. 1980; 17(5):373-9.
PMID: 7218277
PMC: 1048601.
DOI: 10.1136/jmg.17.5.373.
Retardation of ovarian growth in male-sterile mice carrying an autosomal translocation.
MITTWOCH U, Mahadevaiah S, Olive M
J Med Genet. 1981; 18(6):414-7.
PMID: 7199575
PMC: 1048784.
DOI: 10.1136/jmg.18.6.414.
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.
Meiotic studies and synaptonemal complex analysis in two infertile males with a 13/14 balanced translocation.
Templado C, Vidal F, Navarro J, Marina S, Egozcue J
Hum Genet. 1984; 67(2):162-5.
PMID: 6745935
DOI: 10.1007/BF00272992.
Paternal Robertsonian translocation t(13q;14q) and maternal reciprocal translocation t(7p;13q) in a couple with repeated fetal loss.
Scarbrough P, Carroll A, Younger J, Finley S
J Med Genet. 1984; 21(6):463-4.
PMID: 6512837
PMC: 1049349.
DOI: 10.1136/jmg.21.6.463.
Reproductive hormone studies in three subjects with a Robertsonian translocation.
Uccellatore F, Padova G, Squatrito S
J Endocrinol Invest. 1983; 6(6):479-84.
PMID: 6423723
DOI: 10.1007/BF03348348.
XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus).
Forejt J, Gregorova S, Goetz P
Chromosoma. 1981; 82(1):41-53.
PMID: 6167408
DOI: 10.1007/BF00285748.
Nature and consequences of induced chromosome damage in mammals.
SEARLE A
Genetics. 1974; 78(1):173-86.
PMID: 4442701
PMC: 1213177.
DOI: 10.1093/genetics/78.1.173.
Centromere staining at meiosis in man.
CHANDLEY A, Fletcher J
Humangenetik. 1973; 18(3):247-52.
PMID: 4124201
DOI: 10.1007/BF00290604.
Hypospadias and gynecomastia in a male associated with autosomal balanced translocation.
Krishna Murthy D, SHAH V, Chadha A, Murthy S, Desai A
Indian J Pediatr. 1985; 52(417):417-23.
PMID: 4093178
DOI: 10.1007/BF02806634.
Reciprocal translocation t(1;18)(p32;q21) in a patient with some phenotypical anomalies.
Gil R, Lopez-Gines C, Gregori-Romero M, Sanchez M, Pellin A
Hum Genet. 1987; 77(4):384.
PMID: 3692481
DOI: 10.1007/BF00291431.
Trisomy 16q23----qter arising from a maternal t(13;16)(p12;q23): case report and evidence of the reciprocal balanced maternal rearrangement by the Ag-NOR technique.
Savary J, Vasseur F, Manouvrier S, Daudignon A, Lemaire O, Thieuleux M
Hum Genet. 1991; 88(1):115-8.
PMID: 1959917
DOI: 10.1007/BF00204941.
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.