-
1
-
-
20244376329
-
Chromosome 22, trisomy mosaicism
-
Buyse ML (ed). Malden, MA: Blackwell Science, Inc
-
Wertelecki W. Chromosome 22, trisomy mosaicism. In: Buyse ML (ed). Birth Defects Encyclopedia. Malden, MA: Blackwell Science, Inc; 1990:395.
-
(1990)
Birth Defects Encyclopedia
, pp. 395
-
-
Wertelecki, W.1
-
2
-
-
0019198839
-
A cytogenetic study of 1000 spontaneous abortions
-
Hassold T, Chen N, Funkhouser J, et al. A cytogenetic study of 1000 spontaneous abortions. Ann Hum Genet 1980; 44:151-178.
-
(1980)
Ann Hum Genet
, vol.44
, pp. 151-178
-
-
Hassold, T.1
Chen, N.2
Funkhouser, J.3
-
4
-
-
0015097306
-
Trisomy 22: A clinical entity
-
Hsu LY, Shapiro LR, Gertner M, Lieber E, Hirschhorn K. Trisomy 22: a clinical entity. J Pediatr 1971; 79:12-19.
-
(1971)
J Pediatr
, vol.79
, pp. 12-19
-
-
Hsu, L.Y.1
Shapiro, L.R.2
Gertner, M.3
Lieber, E.4
Hirschhorn, K.5
-
5
-
-
0019522231
-
Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction: Delineation of a common clinical picture and report of 9 new cases from 6 families
-
Schinzel A, Schmid W, Auf der Maur P, et al. Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction: delineation of a common clinical picture and report of 9 new cases from 6 families. Hum Genet 1981; 56:249-262.
-
(1981)
Hum Genet
, vol.56
, pp. 249-262
-
-
Schinzel, A.1
Schmid, W.2
Auf der Maur, P.3
-
6
-
-
0019422087
-
Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22
-
Schinzel A. Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22. Hum Genet 1981; 56:269-273.
-
(1981)
Hum Genet
, vol.56
, pp. 269-273
-
-
Schinzel, A.1
-
7
-
-
0028926083
-
Clinical and molecular studies in full trisomy 22: Further delineation of the phenotype and review of the literature
-
Bacino CA, Schreck R, Fischel-Ghodsian N, Pepkowitz S, Prezant TR, Graham JM Jr. Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literature. Am J Med Genet 1995; 56:359-365.
-
(1995)
Am J Med Genet
, vol.56
, pp. 359-365
-
-
Bacino, C.A.1
Schreck, R.2
Fischel-Ghodsian, N.3
Pepkowitz, S.4
Prezant, T.R.5
Graham J.M., Jr.6
-
8
-
-
0030752675
-
Mosaic trisomy 22: A case presentation and literature review of trisomy 22 phenotypes
-
Crowe CA, Schwartz S, Black CJ, Jaswaney V. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes. Am J Med Genet 1997; 71:406-413.
-
(1997)
Am J Med Genet
, vol.71
, pp. 406-413
-
-
Crowe, C.A.1
Schwartz, S.2
Black, C.J.3
Jaswaney, V.4
-
11
-
-
0035169170
-
Extended prenatal survival of a non-mosaic trisomy 22 with aneuploid cytotrophoblasts
-
Hengstschlager M, Bettelheim D, Rosner M, Repa C, Deutinger J, Bernaschek G. Extended prenatal survival of a non-mosaic trisomy 22 with aneuploid cytotrophoblasts. Prenat Diagn 2001; 21:897-899.
-
(2001)
Prenat Diagn
, vol.21
, pp. 897-899
-
-
Hengstschlager, M.1
Bettelheim, D.2
Rosner, M.3
Repa, C.4
Deutinger, J.5
Bernaschek, G.6
-
12
-
-
0024347013
-
Hydrops revisited: Literature review of 1414 cases published in the 1980s
-
Machin GA. Hydrops revisited: literature review of 1414 cases published in the 1980s. Am J Med Genet 1989; 34:366-390.
-
(1989)
Am J Med Genet
, vol.34
, pp. 366-390
-
-
Machin, G.A.1
-
13
-
-
0026701703
-
Trisomy 22 with congenital diaphragmatic hernia and absence of corpus callosum in a liveborn premature infant
-
Kim EH, Cohen RS, Ramachandran P, Mineta AK, Babu VR. Trisomy 22 with congenital diaphragmatic hernia and absence of corpus callosum in a liveborn premature infant. Am J Med Genet 1992; 44:437-438.
-
(1992)
Am J Med Genet
, vol.44
, pp. 437-438
-
-
Kim, E.H.1
Cohen, R.S.2
Ramachandran, P.3
Mineta, A.K.4
Babu, V.R.5
-
15
-
-
0034043485
-
Diaphragmatic hernia and Fryns syndrome phenotype in partial trisomy 22
-
de Beaufort C, Schneider F, Chafai R, Colette JM, Delneste D, Pierquin G. Diaphragmatic hernia and Fryns syndrome phenotype in partial trisomy 22. Genet Couns 2000; 11:181-182.
-
(2000)
Genet Couns
, vol.11
, pp. 181-182
-
-
De Beaufort, C.1
Schneider, F.2
Chafai, R.3
Colette, J.M.4
Delneste, D.5
Pierquin, G.6
-
17
-
-
0036896247
-
Congenital diaphragmatic hernia and hydrops: A lethal association?
-
Sydorak RM, Goldstein R, Hirose S, et al. Congenital diaphragmatic hernia and hydrops: a lethal association? J Pediatr Surg 2002; 37:1678-1680.
-
(2002)
J Pediatr Surg
, vol.37
, pp. 1678-1680
-
-
Sydorak, R.M.1
Goldstein, R.2
Hirose, S.3
|