-
1
-
-
0018959217
-
A synopsis of the human Y chromosome
-
Bühler, E.M. (1980). A synopsis of the human Y chromosome, Hum. Genet., 55, 145-175.
-
(1980)
Hum. Genet.
, vol.55
, pp. 145-175
-
-
Bühler, E.M.1
-
2
-
-
0005818533
-
Clinical and cytologic impact of Y-chromosome abnormalities
-
Sandberg, A.A. (Ed). New York: Alan R. Liss
-
Bühler, E.M. (1985). Clinical and cytologic impact of Y-chromosome abnormalities. In: Sandberg, A.A. (Ed). The Y Chromosome, Part B: Clinical Aspects of Y Chromosome Abnormalities, New York: Alan R. Liss, 61-93.
-
(1985)
The Y Chromosome, Part B: Clinical Aspects of Y Chromosome Abnormalities
, pp. 61-93
-
-
Bühler, E.M.1
-
3
-
-
0019436028
-
Localization of male determining factors in man: A thorough review of structural anomalies of the Y chromosome
-
Davis, R.M. (1981). Localization of male determining factors in man: a thorough review of structural anomalies of the Y chromosome, J. Med. Genet., 18, 161-195.
-
(1981)
J. Med. Genet.
, vol.18
, pp. 161-195
-
-
Davis, R.M.1
-
4
-
-
0021689179
-
Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45,XO/46,XY nf)
-
Gänshirt, D., Pawlowitzki, I.H. (1984). Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45,XO/46,XY nf), Hum. Genet., 67, 241-244.
-
(1984)
Hum. Genet.
, vol.67
, pp. 241-244
-
-
Gänshirt, D.1
Pawlowitzki, I.H.2
-
5
-
-
0020634258
-
The distribution of chromosomal genotypes associated with Turner's syndrome: Livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism
-
Hook, E.B., Warburton, D. (1983). The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism, Hum. Genet., 64, 24-27.
-
(1983)
Hum. Genet.
, vol.64
, pp. 24-27
-
-
Hook, E.B.1
Warburton, D.2
-
6
-
-
0028072677
-
Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases
-
Hsu, L.Y.F. (1994). Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases, Am. J. Med. Genet., 53, 108-140.
-
(1994)
Am. J. Med. Genet.
, vol.53
, pp. 108-140
-
-
Hsu, L.Y.F.1
-
7
-
-
0021634135
-
United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis
-
Hsu, L.Y.F., Perlis, T.E. (1984). United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis, Prenat. Diagn., 4, 97-130.
-
(1984)
Prenat. Diagn.
, vol.4
, pp. 97-130
-
-
Hsu, L.Y.F.1
Perlis, T.E.2
-
8
-
-
0025877323
-
Male development of chromosomally female mice transgenic for SRY
-
Koopman, P., Gubby, J., Vivian, N., Goodfellow, P., Lovell-Gadge, R. (1991). Male development of chromosomally female mice transgenic for SRY, Nature, 351, 117-121.
-
(1991)
Nature
, vol.351
, pp. 117-121
-
-
Koopman, P.1
Gubby, J.2
Vivian, N.3
Goodfellow, P.4
Lovell-Gadge, R.5
-
9
-
-
0026794388
-
The majority of the marker chromosomes in Japanese patients with stigmata of Turner syndrome are derived from Y chromosomes
-
Nagafuchi, S., Tamura, T., Nakahori, Y., Takano, K., Nishi, Y., Iwatani, N., Kitao, M., Hori, Y., Konda, S., Hasegawa, T., Numabe, H., Fujieda, K., Tanaka, T., Hibi, I., Nakagome, Y. (1992). The majority of the marker chromosomes in Japanese patients with stigmata of Turner syndrome are derived from Y chromosomes, Hum. Genet., 89, 590-592.
-
(1992)
Hum. Genet.
, vol.89
, pp. 590-592
-
-
Nagafuchi, S.1
Tamura, T.2
Nakahori, Y.3
Takano, K.4
Nishi, Y.5
Iwatani, N.6
Kitao, M.7
Hori, Y.8
Konda, S.9
Hasegawa, T.10
Numabe, H.11
Fujieda, K.12
Tanaka, T.13
Hibi, I.14
Nakagome, Y.15
-
10
-
-
0026337739
-
PCR detection of distal Yp sequences in an XX true hermaphrodite
-
Nakagome, Y., Seki, S., Fukutani, K., Nagafuchi, S., Nakahori, Y., Tamura, T. (1991). PCR detection of distal Yp sequences in an XX true hermaphrodite, Am. J. Med. Genet., 41, 112-114.
-
(1991)
Am. J. Med. Genet.
, vol.41
, pp. 112-114
-
-
Nakagome, Y.1
Seki, S.2
Fukutani, K.3
Nagafuchi, S.4
Nakahori, Y.5
Tamura, T.6
-
11
-
-
0026083237
-
Molecular cloning and mapping of 10 new probes on the human Y chromosome
-
Nakahori, Y., Tamura, T., Nagafuchi, S., Fujieda, K., Minowada, S., Fukutani, K., Fuse, H., Hayashi, K., Kuroki, Y., Fukushima, Y., Agematsu, K., Kuno, T., Kaneko, S., Yamada, K., Kitagawa, T., Nonomura, M., Fukuda, S., Kusano, M., Onigata, S., Hibi, I., Nakagome, Y. (1991). Molecular cloning and mapping of 10 new probes on the human Y chromosome, Genomics, 9, 765-769.
-
(1991)
Genomics
, vol.9
, pp. 765-769
-
-
Nakahori, Y.1
Tamura, T.2
Nagafuchi, S.3
Fujieda, K.4
Minowada, S.5
Fukutani, K.6
Fuse, H.7
Hayashi, K.8
Kuroki, Y.9
Fukushima, Y.10
Agematsu, K.11
Kuno, T.12
Kaneko, S.13
Yamada, K.14
Kitagawa, T.15
Nonomura, M.16
Fukuda, S.17
Kusano, M.18
Onigata, S.19
Hibi, I.20
Nakagome, Y.21
more..
-
12
-
-
0024571647
-
Three-color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequences
-
Nederlof, P.M., Robinson, D., Abuknesha, R., Wiegant, J., Hopman, A.H.N., Tanke, H.J., Raap, A.K. (1989). Three-color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequences, Cytometry, 10, 20-27.
-
(1989)
Cytometry
, vol.10
, pp. 20-27
-
-
Nederlof, P.M.1
Robinson, D.2
Abuknesha, R.3
Wiegant, J.4
Hopman, A.H.N.5
Tanke, H.J.6
Raap, A.K.7
-
13
-
-
0022992693
-
Sex reversal: Deletion mapping the male-determining function of the human Y chromosome
-
Page, D.C. (1986). Sex reversal: deletion mapping the male-determining function of the human Y chromosome, Cold Spring Harbor Symp. Quant. Biol., 51, 229-235.
-
(1986)
Cold Spring Harbor Symp. Quant. Biol.
, vol.51
, pp. 229-235
-
-
Page, D.C.1
-
14
-
-
0023663890
-
The sex-determining region of the human Y chromosome encodes a finger protein
-
Page, D.C., Mosher, R., Simpson, E.M., Fisher, E.M.C., Mardon, G., Pollack, J., McGillivray, B., de la Chapelle, A., Brown, L.G. (1987). The sex-determining region of the human Y chromosome encodes a finger protein, Cell, 51, 1091-1104.
-
(1987)
Cell
, vol.51
, pp. 1091-1104
-
-
Page, D.C.1
Mosher, R.2
Simpson, E.M.3
Fisher, E.M.C.4
Mardon, G.5
Pollack, J.6
McGillivray, B.7
De La Chapelle, A.8
Brown, L.G.9
-
15
-
-
0022446922
-
Cytogenetic analysis using quantitative, high sensitivity, fluorescence hybridization
-
Pinkel, D., Straume, T., Gray, J.W. (1986). Cytogenetic analysis using quantitative, high sensitivity, fluorescence hybridization, Proc. Natl. Acad. Sci. USA, 83, 2934-2938.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 2934-2938
-
-
Pinkel, D.1
Straume, T.2
Gray, J.W.3
-
16
-
-
0004136246
-
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory
-
Sambrook, J., Fritsch, E.F., Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual, 2nd edn, Cold Spring Harbor, NY: Cold Spring Harbor Laboratory.
-
(1989)
Molecular Cloning: A Laboratory Manual, 2nd Edn
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
17
-
-
0023604923
-
Mapping the H-Y gene
-
Simpson, E., Chandler, P., McLaren, A., Goulmy, E., Disteche, C.M., Page, D.C., Ferguson-Smith, M.A. (1987). Mapping the H-Y gene, Development, 101(Suppl.), 157-161.
-
(1987)
Development
, vol.101
, Issue.SUPPL.
, pp. 157-161
-
-
Simpson, E.1
Chandler, P.2
McLaren, A.3
Goulmy, E.4
Disteche, C.M.5
Page, D.C.6
Ferguson-Smith, M.A.7
-
18
-
-
0025364886
-
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif
-
Sinclair, A.M., Berta, P., Palmer, M.S., Hawkins, J.R., Griffiths, B.L., Smith, D.J., Foster, J.W., Frischauf, A.-M., Lovell-Badge, R., Goodfellow, P.N. (1990). A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif, Nature, 346, 240-244.
-
(1990)
Nature
, vol.346
, pp. 240-244
-
-
Sinclair, A.M.1
Berta, P.2
Palmer, M.S.3
Hawkins, J.R.4
Griffiths, B.L.5
Smith, D.J.6
Foster, J.W.7
Frischauf, A.-M.8
Lovell-Badge, R.9
Goodfellow, P.N.10
-
19
-
-
0023604665
-
Repeated DNA of the human Y chromosome
-
Smith, K.D., Young, K.E., Talbot, C.C., Jr, Schmeckpeper, B.J. (1987). Repeated DNA of the human Y chromosome, Development, 101(Suppl.), 77-92.
-
(1987)
Development
, vol.101
, Issue.SUPPL.
, pp. 77-92
-
-
Smith, K.D.1
Young, K.E.2
Talbot Jr., C.C.3
Schmeckpeper, B.J.4
-
20
-
-
0022530702
-
A deletion map of the human Y chromosome based DNA hybridization
-
Vergnaud, G., Page, D.C., Simmler, M.-C., Brown, L., Rouyer, F., Noel, B., Botstein, D., de la Chapelle, A., Simpson, J.L. (1986). A deletion map of the human Y chromosome based DNA hybridization, Am. J. Hum. Genet., 38, 109-124.
-
(1986)
Am. J. Hum. Genet.
, vol.38
, pp. 109-124
-
-
Vergnaud, G.1
Page, D.C.2
Simmler, M.-C.3
Brown, L.4
Rouyer, F.5
Noel, B.6
Botstein, D.7
De La Chapelle, A.8
Simpson, J.L.9
-
21
-
-
0026756965
-
The human Y chromosome: A 43-interval map based on naturally occurring deletions
-
Vollrath, D., Foote, S., Hilton, A., Brown, L.G., Beer-Romero, P., Bogan, J.S., Page, D.C. (1992). The human Y chromosome: a 43-interval map based on naturally occurring deletions, Science, 258, 52-59.
-
(1992)
Science
, vol.258
, pp. 52-59
-
-
Vollrath, D.1
Foote, S.2
Hilton, A.3
Brown, L.G.4
Beer-Romero, P.5
Bogan, J.S.6
Page, D.C.7
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