-
1
-
-
0029999611
-
Molecular analysis of chromosome 21 in a patient with a phenotype of down syndrome and apparently normal karyotype
-
Ahlbom BE, Goetz P, Korenberg JR, Pettersson U, Seemanova E, Wadelius C, Zech L, Anneren G. 1996. Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype. Am J Med Genet 63: 566-572.
-
(1996)
Am J Med Genet
, vol.63
, pp. 566-572
-
-
Ahlbom, B.E.1
Goetz, P.2
Korenberg, J.R.3
Pettersson, U.4
Seemanova, E.5
Wadelius, C.6
Zech, L.7
Anneren, G.8
-
2
-
-
0030851892
-
A case of apparent trisomy 21 without the down syndrome phenotype
-
Avramopoulos D, Kennerknecht I, Barbi G, Eckert D, Delabar JM, Maunoury C, Hallberg A, Petersen MB. 1997. A case of apparent trisomy 21 without the Down syndrome phenotype. J Med Genet 34: 597-600.
-
(1997)
J Med Genet
, vol.34
, pp. 597-600
-
-
Avramopoulos, D.1
Kennerknecht, I.2
Barbi, G.3
Eckert, D.4
Delabar, J.M.5
Maunoury, C.6
Hallberg, A.7
Petersen, M.B.8
-
3
-
-
0022536322
-
Successful midtrimester thoracocentesis with analysis of the lymphocyte population in the pleural effusion
-
Benacerraf BR, Frigoletto FD Jr, Wilson M. 1986. Successful midtrimester thoracocentesis with analysis of the lymphocyte population in the pleural effusion. Am J Obstet Gynecol 155: 398-399.
-
(1986)
Am J Obstet Gynecol
, vol.155
, pp. 398-399
-
-
Benacerraf, B.R.1
Frigoletto F.D., Jr.2
Wilson, M.3
-
4
-
-
0031977584
-
Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling
-
Berghella V, Wapner RJ, Yang-Feng T, Mahoney MJ. 1998. Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling. Prenat Diagn 18: 384-389.
-
(1998)
Prenat Diagn
, vol.18
, pp. 384-389
-
-
Berghella, V.1
Wapner, R.J.2
Yang-Feng, T.3
Mahoney, M.J.4
-
6
-
-
0025637602
-
Origin of extra chromosome 21 in 343 families: Cytogenic and molecular approaches
-
Dagna-Bricarelli F, Pierluigi M, Grasso M, Strigini P, Perroni L. 1990. Origin of extra chromosome 21 in 343 families: cytogenic and molecular approaches. Am J Med Genet 7 (Suppl.): 129-132.
-
(1990)
Am J Med Genet
, vol.7
, Issue.SUPPL.
, pp. 129-132
-
-
Dagna-Bricarelli, F.1
Pierluigi, M.2
Grasso, M.3
Strigini, P.4
Perroni, L.5
-
7
-
-
0025847724
-
'False-negative' and 'false-positive' prenatal cytogenetic results due to 'true' mosaicism
-
Hammer P, Holzgreve W, Karabacak Z, Horst J, Miny P. 1991. 'False-negative' and 'false-positive' prenatal cytogenetic results due to 'true' mosaicism. Prenat Diagn 11: 133-136.
-
(1991)
Prenat Diagn
, vol.11
, pp. 133-136
-
-
Hammer, P.1
Holzgreve, W.2
Karabacak, Z.3
Horst, J.4
Miny, P.5
-
8
-
-
0024329403
-
Chylothorax in Down syndrome associated with hydrops fetalis
-
Ho NK, Leong MKY, Lim SB. 1989. Chylothorax in Down syndrome associated with hydrops fetalis. J Singapore Paediatr Soc 31: 90-92.
-
(1989)
J Singapore Paediatr Soc
, vol.31
, pp. 90-92
-
-
Ho, N.K.1
Leong, M.K.Y.2
Lim, S.B.3
-
9
-
-
0021709296
-
Investigation of nonimmune hydrops fetalis
-
Holzgreve W, Curry CJ, Golbus MS, Callen PW, Filly RA, Smith JC. 1984. Investigation of nonimmune hydrops fetalis. Am J Obstet Gynecol 150: 805-812.
-
(1984)
Am J Obstet Gynecol
, vol.150
, pp. 805-812
-
-
Holzgreve, W.1
Curry, C.J.2
Golbus, M.S.3
Callen, P.W.4
Filly, R.A.5
Smith, J.C.6
-
10
-
-
0017347991
-
Exclusion of chromosome mosaicism: Tables of 90 percent, 95 percent, and 99 percent confidence limits and comments on use
-
Hook EB. 1977. Exclusion of chromosome mosaicism: tables of 90 percent, 95 percent, and 99 percent confidence limits and comments on use. Am J Hum Genet 29: 94.
-
(1977)
Am J Hum Genet
, vol.29
, pp. 94
-
-
Hook, E.B.1
-
11
-
-
0026537515
-
Hydrops fetalis polyhydramnios, pulmonary hypoplasia and Down syndrome
-
Ilagan NB, Liang KC, Delaney Black V, Perrin E. 1992. Hydrops fetalis polyhydramnios, pulmonary hypoplasia and Down syndrome. Am J Perinatol 9: 9-10.
-
(1992)
Am J Perinatol
, vol.9
, pp. 9-10
-
-
Ilagan, N.B.1
Liang, K.C.2
Delaney Black, V.3
Perrin, E.4
-
12
-
-
0024312714
-
Primary fetal hydrothorax: Natural history and management
-
Longaker MT, Laberge JM, Dansereau J, Langer JC, Crombelholme T, Callen PW, Golbus MS, Harrison MR. 1989. Primary fetal hydrothorax: natural history and management. J Pediatr Surg 24: 573-576.
-
(1989)
J Pediatr Surg
, vol.24
, pp. 573-576
-
-
Longaker, M.T.1
Laberge, J.M.2
Dansereau, J.3
Langer, J.C.4
Crombelholme, T.5
Callen, P.W.6
Golbus, M.S.7
Harrison, M.R.8
-
13
-
-
0029028217
-
Congenital chylothorax with hydrops: Postnatal care and outcome following antenatal diagnosis
-
Mussat P, Dommergues M, Parat S, Mandelbrot L, De Gamarra E, Dumez Y, Moriette G. 1995. Congenital chylothorax with hydrops: postnatal care and outcome following antenatal diagnosis. Acta Paediatr 84: 749-755.
-
(1995)
Acta Paediatr
, vol.84
, pp. 749-755
-
-
Mussat, P.1
Dommergues, M.2
Parat, S.3
Mandelbrot, L.4
De Gamarra, E.5
Dumez, Y.6
Moriette, G.7
-
14
-
-
0022627246
-
Rapid karyotyping in non lethal fetal malformations
-
Nicolaides KH, Rodeck CH, Gosden CM. 1986. Rapid karyotyping in non lethal fetal malformations. Lancet 1: 283-287.
-
(1986)
Lancet
, vol.1
, pp. 283-287
-
-
Nicolaides, K.H.1
Rodeck, C.H.2
Gosden, C.M.3
-
15
-
-
0028036242
-
Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis
-
Pangalos C, Avramopoulos D, Blouin JL, Raoual O, deBlois MC, Prieur M, Schinzel AA, Gika M, Abais D, Antonarakis SE. 1994. Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis. Am J Hum Genet 54: 473-481.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 473-481
-
-
Pangalos, C.1
Avramopoulos, D.2
Blouin, J.L.3
Raoual, O.4
DeBlois, M.C.5
Prieur, M.6
Schinzel, A.A.7
Gika, M.8
Abais, D.9
Antonarakis, S.E.10
-
16
-
-
0028854976
-
Molecular studies of chromosomal mosaicism: Relative frequency of chromosome gain or loss and possible role of cell selection
-
Robinson WP, Binkert F, Bernasconi F, Lorda Sachez I, Werder EA, Schinzel AA. 1995. Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection. Am J Hum Genet 56: 444-451.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 444-451
-
-
Robinson, W.P.1
Binkert, F.2
Bernasconi, F.3
Lorda Sachez, I.4
Werder, E.A.5
Schinzel, A.A.6
-
18
-
-
0029949155
-
Congenital chylothorax in a patient with 21 trisomy syndrome
-
Yamamoto T, Keoda T, Tamura A, Sawada H, Nagata I, Nagath N, Ito T, Mio Y. 1996. Congenital chylothorax in a patient with 21 trisomy syndrome. Acta Paediatr Japan 38: 689-691.
-
(1996)
Acta Paediatr Japan
, vol.38
, pp. 689-691
-
-
Yamamoto, T.1
Keoda, T.2
Tamura, A.3
Sawada, H.4
Nagata, I.5
Nagath, N.6
Ito, T.7
Mio, Y.8
-
19
-
-
0017669997
-
Chylothorax in two mongoloid infants
-
Yoss BS, Lipsitz PJ. 1977. Chylothorax in two mongoloid infants. Clin Genet 12: 357-360.
-
(1977)
Clin Genet
, vol.12
, pp. 357-360
-
-
Yoss, B.S.1
Lipsitz, P.J.2
|