-
1
-
-
0026921276
-
Identification of sex chromosomal abnormalities by fluorescence in situ hybridization
-
Hou JW, Lee ML, Wang TR: Identification of sex chromosomal abnormalities by fluorescence in situ hybridization. Acta Paediatr Sin 1992;33:332-40.
-
(1992)
Acta Paediatr Sin
, vol.33
, pp. 332-340
-
-
Hou, J.W.1
Lee, M.L.2
Wang, T.R.3
-
2
-
-
0026951888
-
Mosaic ring chromosome 13 analyzed by fluorescence in situ hybridization: Report of a case
-
Hou JW, Liu CH, Wang TR, et al: Mosaic ring chromosome 13 analyzed by fluorescence in situ hybridization: report of a case. J Formos Med Assoc 1992;91:1108-11.
-
(1992)
J Formos Med Assoc
, vol.91
, pp. 1108-1111
-
-
Hou, J.W.1
Liu, C.H.2
Wang, T.R.3
-
3
-
-
8044252237
-
Identification of marker chromosomes by fluorescence in situ hybridization and non-fluorescence enzymatic precipitation
-
Hou JW, Wang TR: Identification of marker chromosomes by fluorescence in situ hybridization and non-fluorescence enzymatic precipitation. J Genet Mol Biol 1993;4:6-12.
-
(1993)
J Genet Mol Biol
, vol.4
, pp. 6-12
-
-
Hou, J.W.1
Wang, T.R.2
-
4
-
-
0028395061
-
Molecular cytogenetic studies of children with marker chromosomes
-
Hou JW, Liu CH, Wang TR: Molecular cytogenetic studies of children with marker chromosomes. J Formos Med Assoc 1994;93:205-9.
-
(1994)
J Formos Med Assoc
, vol.93
, pp. 205-209
-
-
Hou, J.W.1
Liu, C.H.2
Wang, T.R.3
-
5
-
-
0028543608
-
Cytogenetic investigations in trisomy 21 with reciprocal 4/9 translocation
-
Hou JW, Wang TR: Cytogenetic investigations in trisomy 21 with reciprocal 4/9 translocation. J Formos Med Assoc 1994;93:958-60.
-
(1994)
J Formos Med Assoc
, vol.93
, pp. 958-960
-
-
Hou, J.W.1
Wang, T.R.2
-
6
-
-
0000477103
-
Enzymatic synthesis of biotin-labeled polynucleotides: Novel nucleic acid affinity probes
-
Langer PR, Waldrop AA, Ward DC: Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes. Proc Natl Acad Sci USA 1981;78: 6633-7.
-
(1981)
Proc Natl Acad Sci USA
, vol.78
, pp. 6633-6637
-
-
Langer, P.R.1
Waldrop, A.A.2
Ward, D.C.3
-
7
-
-
0023692635
-
Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries
-
Lichter P, Cremer T, Borden J, et al: Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum Genet 1988;80:224-34.
-
(1988)
Hum Genet
, vol.80
, pp. 224-234
-
-
Lichter, P.1
Cremer, T.2
Borden, J.3
-
8
-
-
0025911470
-
Chromosomal in situ hybridization after Giemsa banding
-
Klever M, Grond-Ginsbach C, Scherthan H, et al: Chromosomal in situ hybridization after Giemsa banding. Hum Genet 1991;86:484-6.
-
(1991)
Hum Genet
, vol.86
, pp. 484-486
-
-
Klever, M.1
Grond-Ginsbach, C.2
Scherthan, H.3
-
9
-
-
0028022513
-
Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype
-
Mewar R, Harrison W, Weaver DD, et al: Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype. Am J Med Genet 1994;52:178-83.
-
(1994)
Am J Med Genet
, vol.52
, pp. 178-183
-
-
Mewar, R.1
Harrison, W.2
Weaver, D.D.3
-
10
-
-
0029143403
-
Partial trisomy 13q identified by sequential fluorescence in situ hybridization
-
Rao Gopal VVN, Carpenter NJ, Gucsavas M, et al: Partial trisomy 13q identified by sequential fluorescence in situ hybridization. Am J Med Genet 1995;58:50-3.
-
(1995)
Am J Med Genet
, vol.58
, pp. 50-53
-
-
Rao Gopal, V.V.N.1
Carpenter, N.J.2
Gucsavas, M.3
-
11
-
-
0022916035
-
Contiguous gene syndrome: A component of recognizable syndromes
-
Schmickel RD: Contiguous gene syndrome: a component of recognizable syndromes. J Pediatr 1986;109: 231-41.
-
(1986)
J Pediatr
, vol.109
, pp. 231-241
-
-
Schmickel, R.D.1
-
12
-
-
0041658972
-
Duplication of 15q11.2-15q13 in five cases with different phenotypes
-
Rauch LA, Nevin NC: Duplication of 15q11.2-15q13 in five cases with different phenotypes. J Med Genet 1991;28:573-4.
-
(1991)
J Med Genet
, vol.28
, pp. 573-574
-
-
Rauch, L.A.1
Nevin, N.C.2
-
13
-
-
44949281237
-
Clinical application of fluorescence in situ hybridization
-
Tkachuk DC, Pinkel D, Kuo WL, et al: Clinical application of fluorescence in situ hybridization. Genet Anal Tech Appl 1991;8:67-74.
-
(1991)
Genet Anal Tech Appl
, vol.8
, pp. 67-74
-
-
Tkachuk, D.C.1
Pinkel, D.2
Kuo, W.L.3
-
14
-
-
0029059737
-
Molecular cytogenetic studies of duplication 9q32-q34.3 inserted into 9q13
-
Hou JW, Wang TR: Molecular cytogenetic studies of duplication 9q32-q34.3 inserted into 9q13. Clin Genet 1995;48:148-50.
-
(1995)
Clin Genet
, vol.48
, pp. 148-150
-
-
Hou, J.W.1
Wang, T.R.2
-
15
-
-
44949283389
-
Localizing DNA and RNA within nuclei and chromosomes by FISH
-
McNeil JA, Johnson CV, Carter KC, et al: Localizing DNA and RNA within nuclei and chromosomes by FISH. Genet Anal Tech Appl 1991;8:41-58.
-
(1991)
Genet Anal Tech Appl
, vol.8
, pp. 41-58
-
-
McNeil, J.A.1
Johnson, C.V.2
Carter, K.C.3
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