-
1
-
-
0018429347
-
Trisomy 10p due to a de novo t(10p;13p)
-
Aller V, Abrisqueta JA, Pérez-Castillo A, del Mazo J, Martín-Lucas MA, de Torres ML (1979): Trisomy 10p due to a de novo t(10p;13p). Hum Genet 46:129-134.
-
(1979)
Hum Genet
, vol.46
, pp. 129-134
-
-
Aller, V.1
Abrisqueta, J.A.2
Pérez-Castillo, A.3
Del Mazo, J.4
Martín-Lucas, M.A.5
De Torres, M.L.6
-
2
-
-
0017797384
-
Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship
-
Back E, Vogel W, Hertel C, Schuchmann L (1978): Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship. Hum Genet 41:11-17.
-
(1978)
Hum Genet
, vol.41
, pp. 11-17
-
-
Back, E.1
Vogel, W.2
Hertel, C.3
Schuchmann, L.4
-
3
-
-
0016590754
-
Trisomy 10p: A report of two cases due to familial translocation rcp (10;21)(p11;p11)
-
Cantu J-M, Salamanca F, Buentello L, Carnevale A, Armendares S (1975): Trisomy 10p: A report of two cases due to familial translocation rcp (10;21)(p11;p11). Ann Génét 18:5-11.
-
(1975)
Ann Génét
, vol.18
, pp. 5-11
-
-
Cantu, J.-M.1
Salamanca, F.2
Buentello, L.3
Carnevale, A.4
Armendares, S.5
-
5
-
-
0019497598
-
Evidence of gene dosage effect for HK 1 in the red cells of a patient with trisomy 10pter→p13
-
Dallapiccola B, Serena Lungarotti M, Magnani M, Dacha M (1981): Evidence of gene dosage effect for HK 1 in the red cells of a patient with trisomy 10pter→p13. Ann Génét 24:45-47.
-
(1981)
Ann Génét
, vol.24
, pp. 45-47
-
-
Dallapiccola, B.1
Serena Lungarotti, M.2
Magnani, M.3
Dacha, M.4
-
6
-
-
0018185824
-
Brother and sister with trisomy 10p: 46,XY,(22p+)mat; 46,XX,(22p+)mat
-
de Chieri P, Spatuzza E, Bonich JM (1978): Brother and sister with trisomy 10p: 46,XY,(22p+)mat; 46,XX,(22p+)mat. Hum Genet 45:71-75.
-
(1978)
Hum Genet
, vol.45
, pp. 71-75
-
-
De Chieri, P.1
Spatuzza, E.2
Bonich, J.M.3
-
7
-
-
0021153464
-
Trisomy for the short arm of chromosome 10: Report of a new case resulting from segregation of a maternal balanced translocation t(10qter→q11::14p11→qter)
-
Delaroche I, Bruni L, Giannotti A, Giampaolo R, Aebischer ML (1984): Trisomy for the short arm of chromosome 10: Report of a new case resulting from segregation of a maternal balanced translocation t(10qter→q11::14p11→qter). Helv Paediat Acta 39: 161-166.
-
(1984)
Helv Paediat Acta
, vol.39
, pp. 161-166
-
-
Delaroche, I.1
Bruni, L.2
Giannotti, A.3
Giampaolo, R.4
Aebischer, M.L.5
-
10
-
-
0018669589
-
Partial duplication of the short arm of chromosome 10: Karyotype: 46,XX,dup(10p)(pter→p12::p12::p12→qter)
-
Fryns JP, Deroover J, Haegeman J, Van den Berghe H (1979): Partial duplication of the short arm of chromosome 10: Karyotype: 46,XX,dup(10p)(pter→p12::p12::p12→qter). Hum Genet 47:217-220.
-
(1979)
Hum Genet
, vol.47
, pp. 217-220
-
-
Fryns, J.P.1
Deroover, J.2
Haegeman, J.3
Van Den Berghe, H.4
-
13
-
-
0020525469
-
Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10
-
Herva R, Korhonen S, Haapala K, Timonen E (1983): Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10. Clin Genet 24:50-53.
-
(1983)
Clin Genet
, vol.24
, pp. 50-53
-
-
Herva, R.1
Korhonen, S.2
Haapala, K.3
Timonen, E.4
-
14
-
-
0015616643
-
Precise identification of various chromosomal abnormalities
-
Lond
-
Hirschhorn K, Lucas M, Wallace I (1973): Precise identification of various chromosomal abnormalities. Ann Hum Genet (Lond) 36: 375-379.
-
(1973)
Ann Hum Genet
, vol.36
, pp. 375-379
-
-
Hirschhorn, K.1
Lucas, M.2
Wallace, I.3
-
17
-
-
0017327027
-
Partial trisomy 10p and familial translocation t(7;10)(p22;p12)
-
Johnson G. Bachman R, Roed T, Riddervold P (1977): Partial trisomy 10p and familial translocation t(7;10)(p22;p12). Hum Genet 35:353-356.
-
(1977)
Hum Genet
, vol.35
, pp. 353-356
-
-
Bachman R, J.G.1
Roed, T.2
Riddervold, P.3
-
18
-
-
0002644879
-
Embryofetal-perinatal autopsy and placental examination
-
Dimmick JE, Kalousek DK (eds): Philadelphia: JB Lippincott Co
-
Kalousek DK, Baldwin VJ, Dimmick JE, Norman MG, Cimolai N, Andrews A, Paradice B (1992): Embryofetal-perinatal autopsy and placental examination. In Dimmick JE, Kalousek DK (eds): "Developmental Pathology of the Embryo and Fetus." Philadelphia: JB Lippincott Co, pp. 799-824.
-
(1992)
Developmental Pathology of the Embryo and Fetus
, pp. 799-824
-
-
Kalousek, D.K.1
Baldwin, V.J.2
Dimmick, J.E.3
Norman, M.G.4
Cimolai, N.5
Andrews, A.6
Paradice, B.7
-
19
-
-
0028137843
-
Familial 10p trisomy resulting from a maternal pericentric inversion
-
Kozma C, Meck JM (1994): Familial 10p trisomy resulting from a maternal pericentric inversion. Am J Med Genet 49:281-287.
-
(1994)
Am J Med Genet
, vol.49
, pp. 281-287
-
-
Kozma, C.1
Meck, J.M.2
-
20
-
-
0027432978
-
Three cases of dup(10p)del(10q) syndrome resulting from maternal pericentric inversion
-
Kulharya AS, Schneider NR, Wilson GN (1993): Three cases of dup(10p)del(10q) syndrome resulting from maternal pericentric inversion. Am J Med Genet 47:817-819.
-
(1993)
Am J Med Genet
, vol.47
, pp. 817-819
-
-
Kulharya, A.S.1
Schneider, N.R.2
Wilson, G.N.3
-
21
-
-
0019472282
-
Trisomy 10p produced by recombination involving maternal inversion inv(10) (p11q26)
-
Lansky-Shafer SC, Daniel WL, Ruiz L (1981): Trisomy 10p produced by recombination involving maternal inversion inv(10) (p11q26). J Med Genet 18:59-61.
-
(1981)
J Med Genet
, vol.18
, pp. 59-61
-
-
Lansky-Shafer, S.C.1
Daniel, W.L.2
Ruiz, L.3
-
22
-
-
0026612734
-
Combined 10pter→p11 and 18pter→q11 trisomy in a 7-year-old child
-
Lapière J-C, Verloes A, Herens C, Delfortrie J, van Maldergem L, Gillerot Y, Koulischer L (1992): Combined 10pter→p11 and 18pter→q11 trisomy in a 7-year-old child. Genet Couns 3:155-159.
-
(1992)
Genet Couns
, vol.3
, pp. 155-159
-
-
Lapière, J.-C.1
Verloes, A.2
Herens, C.3
Delfortrie, J.4
Van Maldergem, L.5
Gillerot, Y.6
Koulischer, L.7
-
23
-
-
0017819180
-
Partial trisomy 10p in two generations
-
Lurie IW, Lazjuk GI, Gurevich DB, Kravtzova GI, Nedzved MK, Shved IA (1978): Partial trisomy 10p in two generations. Hum Genet 41:235-241.
-
(1978)
Hum Genet
, vol.41
, pp. 235-241
-
-
Lurie, I.W.1
Lazjuk, G.I.2
Gurevich, D.B.3
Kravtzova, G.I.4
Nedzved, M.K.5
Shved, I.A.6
-
24
-
-
0016785506
-
Exclusion gene mapping utilizing patients with chromosome imbalance: The HL-A system as a prototype
-
Magenis RE, Overton K, Wyandt H, Bergstrom T, Hecht F, Lovrien E (1975): Exclusion gene mapping utilizing patients with chromosome imbalance: The HL-A system as a prototype. Humangenetik 27:91-109.
-
(1975)
Humangenetik
, vol.27
, pp. 91-109
-
-
Magenis, R.E.1
Overton, K.2
Wyandt, H.3
Bergstrom, T.4
Hecht, F.5
Lovrien, E.6
-
25
-
-
0017145036
-
Deux cas de trisomie 10p partielle dus a une translocation paternelle t(10;18)(p13;q23)
-
Moric'-Petrovic' S, Lac'a Z', Krajgher A, Milos'evic J (1976): Deux cas de trisomie 10p partielle dus a une translocation paternelle t(10;18)(p13;q23). Ann Génét 19:195-197.
-
(1976)
Ann Génét
, vol.19
, pp. 195-197
-
-
Moric'-Petrovic, S.1
Lac'a, Z.2
Krajgher, A.3
Milos'evic, J.4
-
26
-
-
0016678738
-
Trisomy of the short arm of chromosome 10
-
Nakagome Y, Kobayashi H (1975): Trisomy of the short arm of chromosome 10. J Med Genet 12:412-424.
-
(1975)
J Med Genet
, vol.12
, pp. 412-424
-
-
Nakagome, Y.1
Kobayashi, H.2
-
27
-
-
0006663184
-
A partial 10p trisomy. -46,XY, rec(10),dup p,inv(10)(p13q26)pat
-
Nomoto N, Nagauchi O (1979): A partial 10p trisomy. -46,XY, rec(10),dup p,inv(10)(p13q26)pat-. Jpn J Hum Genet 27:165A.
-
(1979)
Jpn J Hum Genet
, vol.27
-
-
Nomoto, N.1
Nagauchi, O.2
-
28
-
-
0019268196
-
Trisomie partielle (10pter→10q21) et monosome partielle (21pter→21q21) dues a une translocation réciproque familiale équilibrée (10;21) (q21;q21)
-
Obry E, Piussan Ch, Risbourg B, Dutrillaux B (1980): Trisomie partielle (10pter→10q21) et monosome partielle (21pter→21q21) dues a une translocation réciproque familiale équilibrée (10;21) (q21;q21). Ann Génét 23:216-220.
-
(1980)
Ann Génét
, vol.23
, pp. 216-220
-
-
Obry, E.1
Piussan, Ch.2
Risbourg, B.3
Dutrillaux, B.4
-
29
-
-
0025261055
-
Trisomy 10p syndrome owing to maternal pericentric inversion
-
Ohba K, Ohdo S, Sonoda T (1990): Trisomy 10p syndrome owing to maternal pericentric inversion. J Med Genet 27:264-266.
-
(1990)
J Med Genet
, vol.27
, pp. 264-266
-
-
Ohba, K.1
Ohdo, S.2
Sonoda, T.3
-
30
-
-
0021989863
-
Trisomy 10p, due to an unusual translocation
-
Orye E, Van Haesebrouck P, Van Coster R, Van Mele B (1985): Trisomy 10p, due to an unusual translocation. J Genet Hum 33: 63-66.
-
(1985)
J Genet Hum
, vol.33
, pp. 63-66
-
-
Orye, E.1
Van Haesebrouck, P.2
Van Coster, R.3
Van Mele, B.4
-
31
-
-
0017748235
-
Trisomy for the short arm of chromosome No. 10
-
Penchaszadeh VB, Coco R (1977): Trisomy for the short arm of chromosome No. 10. J Génét Hum 25:221-227.
-
(1977)
J Génét Hum
, vol.25
, pp. 221-227
-
-
Penchaszadeh, V.B.1
Coco, R.2
-
32
-
-
0026516889
-
Isochromosome/duplication of 10p and translocation of 10q
-
Rivera H, Rivas F (1992): Isochromosome/duplication of 10p and translocation of 10q. Am J Med Genet 42:396-397.
-
(1992)
Am J Med Genet
, vol.42
, pp. 396-397
-
-
Rivera, H.1
Rivas, F.2
-
33
-
-
0024321939
-
A case of two inversion (10) recombinants in a family
-
Roberts P, Williams J, Sills MA (1989): A case of two inversion (10) recombinants in a family. J Med Genet 26:461-464.
-
(1989)
J Med Genet
, vol.26
, pp. 461-464
-
-
Roberts, P.1
Williams, J.2
Sills, M.A.3
-
34
-
-
0018570481
-
La trisomie 10p: Étude clinique et biochimique
-
Rochon M, Powell J, Blanchard R, Paré C, Lemieux B (1979): La trisomie 10p: étude clinique et biochimique. L'Union Méd Canada 108:1490-1493.
-
(1979)
L'Union Méd Canada
, vol.108
, pp. 1490-1493
-
-
Rochon, M.1
Powell, J.2
Blanchard, R.3
Paré, C.4
Lemieux, B.5
-
35
-
-
0017666632
-
Trisomie 10p partielle d'origine paternelle deux nouvelles observations dans deux familles différentes
-
Rolland M, Bourrouillou G, Elana G, Colombies P, Regnier C (1977): Trisomie 10p partielle d'origine paternelle deux nouvelles observations dans deux familles différentes. Ann Génét 20: 209-213.
-
(1977)
Ann Génét
, vol.20
, pp. 209-213
-
-
Rolland, M.1
Bourrouillou, G.2
Elana, G.3
Colombies, P.4
Regnier, C.5
-
36
-
-
0016156825
-
C bands in human metaphase chromosome treated with barium hydroxide
-
Salamanca F, Armendares S (1974): C bands in human metaphase chromosome treated with barium hydroxide. Ann Génét 17: 135-136.
-
(1974)
Ann Génét
, vol.17
, pp. 135-136
-
-
Salamanca, F.1
Armendares, S.2
-
37
-
-
0016185109
-
Brother and sister with trisomy 10p: A new syndrome
-
Schleiermacher E, Schliebitz U, Steffens C, Rompe G, Schmidt U (1974): Brother and sister with trisomy 10p: A new syndrome. Humangenetik 23:163-172.
-
(1974)
Humangenetik
, vol.23
, pp. 163-172
-
-
Schleiermacher, E.1
Schliebitz, U.2
Steffens, C.3
Rompe, G.4
Schmidt, U.5
-
38
-
-
0021202479
-
Duplication of chromosome 10p: Confirmation of regional assignments of platelet-type phosphofructokinase
-
Schwartz S, Cohen MM, Fanny SR, Beisel JH, Vora S (1984): Duplication of chromosome 10p: Confirmation of regional assignments of platelet-type phosphofructokinase. Am J Hum Genet 36: 750-759.
-
(1984)
Am J Hum Genet
, vol.36
, pp. 750-759
-
-
Schwartz, S.1
Cohen, M.M.2
Fanny, S.R.3
Beisel, J.H.4
Vora, S.5
-
39
-
-
0015246254
-
A rapid banding technique for human chromosomes
-
Seabright M (1971): A rapid banding technique for human chromosomes. Lancet 2:971-972.
-
(1971)
Lancet
, vol.2
, pp. 971-972
-
-
Seabright, M.1
-
40
-
-
0028345640
-
Ophthalmic findings in partial monosomy 4p (Wolf syndrome) in combination with partial trisomy 10p
-
Seiberth V, Kachel W, Knorz MC, Liesenhoff H (1994): Ophthalmic findings in partial monosomy 4p (Wolf syndrome) in combination with partial trisomy 10p. Am J Ophthalmol 117:411-413.
-
(1994)
Am J Ophthalmol
, vol.117
, pp. 411-413
-
-
Seiberth, V.1
Kachel, W.2
Knorz, M.C.3
Liesenhoff, H.4
-
41
-
-
0024267642
-
Organ weight standards for human fetuses
-
Shepard TH, Shi M, Fellingham GW, Fujinaga M, FitzSimmons JM, Fantel AG, Barr M (1988): Organ weight standards for human fetuses. Pediatr Pathol 8:513-524.
-
(1988)
Pediatr Pathol
, vol.8
, pp. 513-524
-
-
Shepard, T.H.1
Shi, M.2
Fellingham, G.W.3
Fujinaga, M.4
Fitzsimmons, J.M.5
Fantel, A.G.6
Barr, M.7
-
42
-
-
0020375303
-
Two chromosomal syndromes in the same family: Monosomy and trisomy for part of the short arm of chromosome 10
-
Slinde S, Hansteen IL (1982): Two chromosomal syndromes in the same family: Monosomy and trisomy for part of the short arm of chromosome 10. Eur J Pediatr 139:153-157.
-
(1982)
Eur J Pediatr
, vol.139
, pp. 153-157
-
-
Slinde, S.1
Hansteen, I.L.2
-
43
-
-
0021240891
-
A de novo case of trisomy 10p: Gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase
-
Snyder FF, Lin CC, Rudd NL, Shearer JE, Heikkila EM, Hoo JJ (1984): A de novo case of trisomy 10p: Gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase. Hum Genet 67:187-189.
-
(1984)
Hum Genet
, vol.67
, pp. 187-189
-
-
Snyder, F.F.1
Lin, C.C.2
Rudd, N.L.3
Shearer, J.E.4
Heikkila, E.M.5
Hoo, J.J.6
-
44
-
-
0017759883
-
New chromosomal dysmorphic syndromes. 2. Trisomy 10p
-
Stengel-Rutkowski S, Murken JD, Frankenberger R, Riechert M, Spiess H, Rodewald A, Stene J (1977): New chromosomal dysmorphic syndromes. 2. Trisomy 10p. Eur J Pediatr 126:109-125.
-
(1977)
Eur J Pediatr
, vol.126
, pp. 109-125
-
-
Stengel-Rutkowski, S.1
Murken, J.D.2
Frankenberger, R.3
Riechert, M.4
Spiess, H.5
Rodewald, A.6
Stene, J.7
-
45
-
-
0019110905
-
La trisomie 10p. A propos d'une observation due a une translocation maternelle
-
Stoll C, Willard D (1980): La trisomie 10p. A propos d'une observation due a une translocation maternelle. Pediatrie 35:251-255.
-
(1980)
Pediatrie
, vol.35
, pp. 251-255
-
-
Stoll, C.1
Willard, D.2
-
48
-
-
0020607562
-
The origin of inverted tandem duplications, and phenotypic effects of tandem duplication of the X chromosome long arm
-
Van Dyke DL, Miller MJ, Weiss L (1983): The origin of inverted tandem duplications, and phenotypic effects of tandem duplication of the X chromosome long arm. Am J Med Genet 15:441-450.
-
(1983)
Am J Med Genet
, vol.15
, pp. 441-450
-
-
Van Dyke, D.L.1
Miller, M.J.2
Weiss, L.3
-
49
-
-
0022462384
-
A patient with dup(10p)del(8q) and Pendred syndrome
-
van Wouwe JP, Wijnands MC, Mourad-Baars PEC, Geraedts JPM, Beverstock GC, van de Kamp JJP. (1986): A patient with dup(10p)del(8q) and Pendred syndrome. Am J Med Genet 24: 211-217.
-
(1986)
Am J Med Genet
, vol.24
, pp. 211-217
-
-
Van Wouwe, J.P.1
Wijnands, M.C.2
Mourad-Baars, P.E.C.3
Geraedts, J.P.M.4
Beverstock, G.C.5
Van De Kamp, J.J.P.6
-
50
-
-
0014760587
-
A case of multiple congenital anomalies with familial C-G translocation
-
Yanagisawa S, Adachi K (1970): [A case of multiple congenital anomalies with familial C-G translocation.] [Jpn J Hum Genet] 14:309-315.
-
(1970)
Jpn J Hum Genet
, vol.14
, pp. 309-315
-
-
Yanagisawa, S.1
Adachi, K.2
-
51
-
-
0019482437
-
Duplication deficiency as the result of meiotic segregation of a maternal inv(10)
-
Yunis E, Torres de Caballero OT (1981): Duplication deficiency as the result of meiotic segregation of a maternal inv(10). Hum Genet 57:71-74.
-
(1981)
Hum Genet
, vol.57
, pp. 71-74
-
-
Yunis, E.1
Torres De Caballero, O.T.2
|