Segregation patterns and phenotypes of unbalanced offspring in a large family with (10;18) chromosome translocation.
暂无分享,去创建一个
[1] D. Borgaonkar,et al. Segregation analysis in reciprocal translocation carriers. , 1984, American journal of medical genetics.
[2] K. Hansen,et al. Five generations of t(4;8)(q35;q13) leading to a case of partial 8q trisomy with consideration of potential pregnancy outcomes from translocation carriers , 1984, Clinical genetics.
[3] A. Schinzel,et al. Catalogue of Unbalanced Chromosome Aberrations in Man , 1985 .
[4] L. Larson,et al. Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and deletion 10q , 1982, Clinical genetics.
[5] A. Smith,et al. A severely retarded male with deletion of chromosomes 15 (pter leads to q13) and 10 (q 26 leads to qter). , 1982, Journal of medical genetics.
[6] S. Stengel-Rutkowski,et al. Genetic risks for familial reciprocal translocations with special emphasis on those leading to 9p, 10p and 12p trisomies , 1982, Annals of human genetics.
[7] W. Wilson,et al. 18p— syndrome with a single central maxillary incisor , 1981, Journal of medical genetics.
[8] J. Egozcue,et al. Meiotic behaviour of two human reciprocal translocations. , 1981, Journal of medical genetics.
[9] M. L. Podoplelova,et al. Non-homologue pairing and spontaneous meiotic interchanges in Drosophila melanogaster females. , 1981, Mutation research.
[10] R. Verma,et al. Double trisomy 48,XXX,+ 18 in a newborn. , 1981, American journal of medical genetics.
[11] C. Turleau,et al. Trisomy 18q‐. Trisomy mapping of chromosome 18 revisited , 1980, Clinical genetics.
[12] E. Zackai,et al. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction. , 1980, American journal of medical genetics.
[13] B. Sele,et al. Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations. , 1979, Journal of medical genetics.
[14] R. Sparkes,et al. 47,XX,+der(18),t(9;18)(p24;q21) mat: a distinct partial trisomy 18q--syndrome? , 1978, Journal of medical genetics.
[15] R. C. Lewandowski,et al. Abnormalities resulting from a familial pericentric inversion of chromosome 18 , 1978, Clinical genetics.
[16] D. Coleman,et al. Partial trisomy 18 in a family with a translocation (18;21)(q21;q22). , 1978, Journal of medical genetics.
[17] S. Jalal,et al. Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation. , 1978, Journal of medical genetics.
[18] C. Turleau,et al. Trisomy 18qter and trisomy mapping of chromosome 18 , 1977, Clinical genetics.
[19] T. E. Denton,et al. Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18. , 1976, Journal of medical genetics.
[20] J. Yunis. High resolution of human chromosomes. , 1976, Science.
[21] L. Stern,et al. Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat. , 1975, Journal of medical genetics.
[22] M. Bobrow,et al. Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring. , 1975, Journal of medical genetics.
[23] M. Steele,et al. Trisomy for the distal half of the long arm of chromosome no. 18. A report of two affected sibs. , 1974, The Journal of pediatrics.
[24] J. Hamerton,et al. Familial mental retardation in a family with an inherited chromosome rearrangement , 1974, Journal of medical genetics.
[25] R. Grell,et al. Distributive Pairing and Aneuploidy in Man , 1964, Science.