Reciprocal translocations: A way to predict the mode of imbalanced segregation by pachytene-diagram drawing

[1]  Yoshifumi Yamamoto,et al.  Partial trisomy of 11 and 22 due to familial translocation t(11;22) (q23;q11), inherited in three generations , 1979, Human Genetics.

[2]  A. Daniel.  Structural differences in reciprocal translocations , 1979, Human Genetics.

[3]  D. Kurnit.  Satellite DNA and heterochromatin variants: The case for unequal mitotic crossing over , 1979, Human Genetics.

[4]  E. Yunis,et al.  Partial trisomy-5p , 1978, Human Genetics.

[5]  J. Faust,et al.  Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11) , 1978, Human Genetics.

[6]  G. Lazjuk,et al.  Partial trisomy 10p in two generations , 1978, Human Genetics.

[7]  W. Vogel,et al.  Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship , 1978, Human Genetics.

[8]  N. Archidiacono,et al.  t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring , 1978, Human Genetics.

[9]  A. Mcdermott,et al.  Cri-du-chat Syndrome in a child with a 46,XX,der(5),t(4;5)(q32;p14)pat karyotype , 1977, Human Genetics.

[10]  E. Yunis,et al.  Partial trisomy 16q- , 1977, Human Genetics.

[11]  M. Breuning,et al.  Partial trisomy 6p due to familial translocation t(6;20)(p21;p13) , 1977, Human Genetics.

[12]  R. Pfeiffer,et al.  47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat , 1977, Human Genetics.

[13]  J. Fryns,et al.  Partial trisomy 14q due to familial t(14q-, 11q+) translocation , 1977, Human Genetics.

[14]  C. Turleau,et al.  Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers , 1977, Human Genetics.

[15]  R. Bachman,et al.  Partial trisomy 10p and familial translocation t(7;10)(p22;p12) , 1977, Human Genetics.

[16]  E. Reske‐Nielsen,et al.  A newborn child with karyotype 47,XX,+der(12) (12pter→12q12::8q24→8qter),t(8;12) (q24;q12) pat , 1977, Human Genetics.

[17]  U. Francke,et al.  Partial trisomy 20p derived from a t(18;20) translocation , 1976, Human Genetics.

[18]  T. Bauknecht,et al.  Trisomy 4p due to a paternal t(4p-;16p+) translocation , 1976, Human Genetics.

[19]  R. Bachman,et al.  A 46, XY, del(18)(pter→pl 100:) Cebocephalic child from a 46, XX, t(12;18)(18pter→18pl 100 :: 12qter→12pter) normal parent , 1976, Human Genetics.

[20]  R. Gorlin,et al.  Partial trisomy 4q syndrome: Case report and review , 1976, Human Genetics.

[21]  E. Juillard,et al.  A new case of trisomy for the distal part of 13q due to maternal translocation, t(9;13)(p21;q21) , 1976, Human Genetics.

[22]  S. R. Young,et al.  Tertiary trisomy, 47,XX,+14q-, resulting from maternal balanced translocation, 46,XX,t(14;16)(q11;q24) , 1976, Human Genetics.

[23]  A. Rett,et al.  Two cases of trisomy 4p with translocation t(4p-,7q+) in several members of one family , 1976, Human Genetics.

[24]  P. Bowen,et al.  Partial trisomy 4q due to familial 2/4 translocation , 1976, Human Genetics.

[25]  R. Pfeiffer,et al.  Partial trisomy 15q1 , 1976, Human Genetics.

[26]  J. Nielsen,et al.  A family with a high risk of segregation for an autosomal unbalanced reciprocal translocation , 1976, Human Genetics.

[27]  I. Šubrt,et al.  Trisomy 9p resulting from maternal 9/21 translocation , 1976, Human Genetics.

[28]  A. Schinzel,et al.  Further delineation of the clinical picture of trisomy for the distal segment of chromosome 13 , 1976, Human Genetics.

[29]  B. Zabel,et al.  Partial trisomy 2q and familial translocation t(2;12)(q31;q24) , 1976, Human Genetics.

[30]  J. Zizka,et al.  A case of trisomy 9p in a family with translocation 9/15 , 1975, Humangenetik.

[31]  R. Phillips.  Inheritance of acrocentric association patterns , 1975, Humangenetik.

[32]  F. Giraud,et al.  Trisomie partielle 11q et translocation familiale 11–22 , 1975, Humangenetik.

[33]  D. Schiff,et al.  Partial trisomy 12p due to t(12;21)pat translocation , 2004, Human Genetics.

[34]  C. Stoll,et al.  Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13) , 2004, Humangenetik.

[35]  B. Sele,et al.  Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations. , 1979, Journal of medical genetics.

[36]  P. Jacobs,et al.  Direct analysis of the chromosome constitution of human spermatozoa , 1978, Nature.

[37]  B. Noel,et al.  7 cases of trisomy 2q 34 to 2q ter resulting from a familial translocation 2 8 q 34 p 23 , 1978 .

[38]  I. Hansteen,et al.  Trisomy 12p syndrome Evaluation of a family with a t(12;21)(p12.1;p11) translocation with unbalanced offspring , 1978, Clinical genetics.

[39]  B. Zabel,et al.  Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes. , 1978, Journal of medical genetics.

[40]  D. Coleman,et al.  Partial trisomy 18 in a family with a translocation (18;21)(q21;q22). , 1978, Journal of medical genetics.

[41]  B. Crandall,et al.  A 45,XX,-5,-14,+t(5q;14q)mat cri du chat child. , 1978, Annales de genetique.

[42]  M. Cohen,et al.  Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11). , 1978, Annales de genetique.

[43]  S. Jalal,et al.  Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation. , 1978, Journal of medical genetics.

[44]  F. Salamanca-Gómez,et al.  Partial 2p trisomy (p21→pter) in two siblings of a family with a 2p‐:15q+ translocation , 1978 .

[45]  P. Guibaud,et al.  Sept cas de trisomie 2q34 leads to 2qter par transmission familiale d'une translocation t(2;8)(q34;p23). , 1978 .

[46]  B. Dallapiccola,et al.  Trisomy 4p: five new observations and overview , 1977, Clinical genetics.

[47]  D. Perl,et al.  Partial trisomy 8 (trisomy 8q2106 leads to 8qter). , 1977, Journal of medical genetics.

[48]  E. Yunis,et al.  Partial trisomy 4q. , 1977, Annales de genetique.

[49]  J. Yunis,et al.  Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3). , 1977, Journal of medical genetics.

[50]  B. Zabel,et al.  [Partial trisomy for the distal part of the long arm of chromosome 15 due to a balanced maternal X/15 tranlsocation]. , 1977, Annales de genetique.

[51]  R. Liersch,et al.  Partial duplication 5q syndrome: phenotypic similarity in two sisters with identical karyotype (partial duplication 5q33 leads to 5qter and partial deficiency 8p23 leads to pter). , 1977, Annales de genetique.

[52]  W. Gooch,et al.  Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family. , 1977, Annales de genetique.

[53]  C. Turleau,et al.  Trisomy 18qter and trisomy mapping of chromosome 18 , 1977, Clinical genetics.

[54]  V. Penchaszadeh,et al.  Trisomy for the short arm of chromosome No. 10. , 1977, Journal de genetique humaine.

[55]  M. Mattei,et al.  [Partial trisomy 13 due to maternal translocation t(2;13)]. , 1977, Annales de genetique.

[56]  M. Rolland,et al.  [Partial trisomy 10p of paternal origin. 2 new cases in 2 different families]. , 1977, Annales de genetique.

[57]  F. Brimblecombe,et al.  'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations. , 1977, Journal of medical genetics.

[58]  L. Larson,et al.  Partial trisomy 7p associated with familial 7p;22q translocation. , 1977, Journal of medical genetics.

[59]  P. Garlinger,et al.  Partial trisomy 22: A recognizable syndrome , 1977, Clinical genetics.

[60]  G. Schwanitz,et al.  [Familial translocation 3/22 MAT with partial trisomy 3q (author's transl)]. , 1977, Journal de genetique humaine.

[61]  U. Francke,et al.  Familial trisomy 20p five cases and two carriers in three generations a review. , 1977, Annales de genetique.

[62]  F. Freycon,et al.  [Two new cases of trisomy 10q21 to 10qter in two sisters due to paternal translocation t(9;10) (q34;q24)]. , 1977, Annales de genetique.

[63]  H. Zellweger,et al.  Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature. , 1977, Journal of medical genetics.

[64]  U. Francke,et al.  Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat. , 1977, Annales de genetique.

[65]  J. Hemet,et al.  [Trisomy 9p by mat. t(2;9)(q36;q31)]. , 1977, Annales de genetique.

[66]  V. Penchaszadeh,et al.  Partial trisomy 14q and familial translocation (2;14) (q12;q13). , 1977, Annales de genetique.

[67]  K. Fried,et al.  Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation. , 1977, Journal of medical genetics.

[68]  R. Pfeiffer,et al.  Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21 , 1977, Clinical genetics.

[69]  O. Zuffardi,et al.  The 9p‐ deletion syndrome A patient with a 45,XX,‐9,‐15, + t(9/15) constitution due to maternal 3:l meiotic disjunction , 1977, Clinical genetics.

[70]  J. Rary,et al.  Translocation 9q/13q resulting in duplication (trisomy 9pter→9q22) and deficiency (monosomy 13pter→13q12) , 1977 .

[71]  R. Berger,et al.  Partial 7q trisomy , 1977, Clinical genetics.

[72]  Hoo Jj.  12P trisomy: a syndrome? , 1976 .

[73]  Y. Nakagome,et al.  A case of partial trisomy 3q , 1976, Journal of medical genetics.

[74]  J. Sills,et al.  Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q. , 1976, Journal of medical genetics.

[75]  B. Dutrillaux,et al.  [Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)]. , 1976, Annales de genetique.

[76]  J. Milośevic,et al.  [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)]. , 1976, Annales de genetique.

[77]  C. Goday,et al.  Cri du chat syndrome and translocation t(5p--;18p+). , 1976, Journal de genetique humaine.

[78]  C. Blank,et al.  Multiple congenital defects associated with trisomy for long arm of No. 4. , 1976, Journal of medical genetics.

[79]  L. Boyd,et al.  Reciprocal translocation, 4q-; 21p+, giving rise to Down's syndrome. , 1976, Journal of medical genetics.

[80]  M. Rethoré,et al.  Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations , 1976, Clinical genetics.

[81]  M. Rethoré,et al.  [Partial trisomy of the long arm of the chromosme 11 by malsegregation of a maternal translocation t(11;22)(q23 1;q1 11)]. , 1976, Annales de genetique.

[82]  S. Morić-Petrović,et al.  [Reciprocal translocation in the family of 2 prositas with partial trisomy of the chromosome 7q]. , 1976, Annales de genetique.

[83]  N. Ayraud,et al.  [Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case]. , 1976, Annales de genetique.

[84]  D. Rivière,et al.  [Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)]. , 1976, Annales de genetique.

[85]  J. German,et al.  De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation. , 1976, Annales de genetique.

[86]  C. Turleau,et al.  [Trisomy 10 p. A previously reported case explained by binding]. , 1976, Annales de genetique.

[87]  O. Alfi,et al.  Trisomy 19 q. , 1976, Annales de genetique.

[88]  A. A. Saadi,et al.  Partial trisomy of the long arm of chromosome 7 , 1976, Clinical genetics.

[89]  W. Centerwall,et al.  Familial 'partial 9p' trisomy: six cases and four carriers in three generations. , 1976, Journal of medical genetics.

[90]  J. Hamerton,et al.  Tertiary trisomy 14: is there a syndrome? , 1976, Birth defects original article series.

[91]  F. Anglani,et al.  Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation. , 1975, Journal of medical genetics.

[92]  Y. Nakagome,et al.  Trisomy of the short arm of chromosome 10. , 1975, Journal of medical genetics.

[93]  B. Dutrillaux,et al.  [Trisomy 10q24--10qter]. , 1975, Annales de genetique.

[94]  M. Seabright,et al.  A family with an inherited translocation involving the no. 4/no. 21 chromosomes. , 1975, Journal of medical genetics.

[95]  S. Finley,et al.  Fetal loss and familial chromosome I translocations * , 1975, Clinical genetics.

[96]  H. Verhaaren,et al.  The 9p‐ deletion syndrome. Report of a patient with a 46, XX, 9p‐ constitution due to a paternal t(9p‐; 15q+) translocation , 1975, Clinical genetics.

[97]  N. Morton,et al.  The effect of structural aberrations of the chromosomes on reproductive fitness in man , 1975, Clinical genetics.

[98]  A. Aurias,et al.  [2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families]. , 1975, Annales de genetique.

[99]  M. Bethenod,et al.  [2 cases of trisomy 11q(q23.2-- qter) with the same abnormality of external genitalia]. , 1975, Annales de genetique.

[100]  D. A. Spencer,et al.  A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-). , 1975, Journal of medical genetics.

[101]  R. Coco,et al.  Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-). , 1975, Journal of medical genetics.

[102]  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.

[103]  M. Mulcahy,et al.  The 9p trisomy syndrome: Two further cases arising from different familial translocations , 1975, Clinical genetics.

[104]  M. Osztovics,et al.  Familial translocation, t(2;5)(p23;q31) , 1975, Clinical genetics.

[105]  C. Junien,et al.  [Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)]. , 1975, Annales de genetique.

[106]  J. Cantú,et al.  The 12p trisomy syndrome. , 1975, Annales de genetique.

[107]  A. Ornoy,et al.  An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15. , 1975, Annales de genetique.

[108]  C. Blank,et al.  Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9 , 1975, Clinical genetics.

[109]  Y. Kuroki,et al.  Two cases of 8p trisomy in one sibship , 1975, Clinical genetics.

[110]  E. Joosten,et al.  Trisomy 4p in a family with A t(4;15). , 1975, Annales de genetique.

[111]  J. Lejeune,et al.  [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)]. , 1975, Annales de genetique.

[112]  M. Bobrow,et al.  Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring. , 1975, Journal of medical genetics.

[113]  E. Niebuhr,et al.  Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23). , 1975, Annales de genetique.

[114]  B. Dutrillaux,et al.  Partial 4q trisomy. Apropos of 3 cases. , 1975, Annales de genetique.

[115]  A. Carnevale,et al.  Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII). , 1975, Annales de genetique.

[116]  F. Bocquentin,et al.  [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)]. , 1975, Annales de genetique.

[117]  R. G. Davidson,et al.  A familial F/G translocation [t(20p‐; 22q+)] observed in three generations , 1975, Clinical genetics.

[118]  F. Ballesta,et al.  [Partial trisomy for the distal part of the short branch of chromosome 3]. , 1974, Annales de genetique.

[119]  J. Scheres,et al.  Trisomy for the short arm of chromosome No. 10 , 1974, Clinical genetics.

[120]  B. Dutrillaux,et al.  [Trisomy 9p gy t(4; 9) (q 34; q21) mat]. , 1974, Annales de genetique.

[121]  J. Messer,et al.  [Equilibrated 2-14 translocation in a mother and partial trisomy of a pair of the short branches of a number 2 chromosome in 2 of her children]. , 1974, Annales de genetique.

[122]  C. Turleau,et al.  [Trisomy 9p : 2 further cases]. , 1974, Annales de genetique.

[123]  M. Mikkelsen,et al.  Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother , 1974, Journal of medical genetics.

[124]  H. Rott,et al.  Partial trisomy 9 in the case of familial translocation 8/9 mat. , 1974, Annales de genetique.

[125]  B. Weisskopf,et al.  Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15p+;9q−) in three generations , 1974 .

[126]  B. Dutrillaux,et al.  [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters]. , 1974, Annales de genetique.

[127]  U. Francke,et al.  Translocation, t(4q−;13q+), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation , 1974 .

[128]  J. Taillemite,et al.  [Partial trisomy 10q dueto familial translocation t(10q-; 22p-plus)]. , 1974, Annales de genetique.

[129]  T. Kajii,et al.  Chromosome anomalies in three successive abortuses due to paternal translocation, t(13q-18q+). , 1974, Cytogenetics and cell genetics.

[130]  W. R. Breg,et al.  Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus). , 1974, Journal of medical genetics.

[131]  A. Chapelle,et al.  Segregating Reciprocal (4;21) (q21;q21) Translocation with Proposita Trisomic for Parts of 4q and 21 , 1973, Journal of medical genetics.

[132]  B. Dutrillaux,et al.  [T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter]. , 1973, Annales de genetique.

[133]  B. Dutrillaux,et al.  [Familial balanced translocation t(2; 13) (q32; q33) and partial trisomy 2q]. , 1973, Annales de genetique.

[134]  B. Dutrillaux,et al.  [Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21]. , 1973, Annales de genetique.

[135]  G. Schwanitz,et al.  Partial trisomy 4p with translocation 4p-, 22p+ in the father. , 1973, Annales de genetique.

[136]  W. Vogel,et al.  Partial trisomy 7q. , 1973, Annales de genetique.

[137]  H. Evans.  Molecular architecture of human chromosomes. , 1973, British medical bulletin.

[138]  G. Donnell,et al.  Partial Trisomy of the Long Arm of Chromosome No. 7 , 1973, Journal of medical genetics.

[139]  Y. Nakagome,et al.  Three Translocations Involving C- or G-group Chromosomes , 1973, Journal of medical genetics.

[140]  B. Dutrillaux,et al.  [Giemsa-R-banding analysis of the trisomy 9p and report of a new case]. , 1973, Humangenetik.

[141]  G. Sutherland,et al.  Partial trisomy of 7q resulting from a familial translocation. , 1973, Annales de genetique.

[142]  W. R. Breg,et al.  A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother. , 1972, Journal of medical genetics.

[143]  J. Opitz,et al.  A case of partial (9p) trisomy in a family with a balanced translocation , 2022 .

[144]  A. Murch.  Pseudohermaphroditism with clinical features of trisomy 18 in an infant trisomic for parts of chromosomes 16 and 18 , 2022 .