-
1
-
-
0002314552
-
Cystic fibrosis
-
Scriver, C.R., Beaudet, A.L., Sly, W.S. and Valle, D. (eds). McGraw-Hill, New York, NY
-
Boat, T.F., Welsh, M.J. and Beaudet, A.L. (1989) Cystic fibrosis. In Scriver, C.R., Beaudet, A.L., Sly, W.S. and Valle, D. (eds). The Metabolic Basis of Inherited Disease, 6th edn, McGraw-Hill, New York, NY, Vol. 2, pp. 2649-2680.
-
(1989)
The Metabolic Basis of Inherited Disease, 6th Edn
, vol.2
, pp. 2649-2680
-
-
Boat, T.F.1
Welsh, M.J.2
Beaudet, A.L.3
-
2
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem, B., Rommens, J.M., Buchanan, J.A., Markiewicz, D.A., Cox, T.K., Chakravarti, A., Buchwald, M. and Tsui, L.-C. (1989) Identification of the cystic fibrosis gene: genetic analysis. Science, 245, 1073-1080.
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
Rommens, J.M.2
Buchanan, J.A.3
Markiewicz, D.A.4
Cox, T.K.5
Chakravarti, A.6
Buchwald, M.7
Tsui, L.-C.8
-
3
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary cDNA
-
Riordan, J.R., Rommens, J.M., Kerem, B.-S., Alon, N., Rozmahel, R., Grzelczak, Z., Zielenski, J., Lok, S., Plavsic, N., Chou, J.-L., Drumm, M.L., Iannuzzi, M.C., Collins, F.S. and Tsui, L.-C. (1989) Identification of the cystic fibrosis gene: cloning and characterization of complementary cDNA. Science, 245, 1066-1073.
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kerem, B.-S.3
Alon, N.4
Rozmahel, R.5
Grzelczak, Z.6
Zielenski, J.7
Lok, S.8
Plavsic, N.9
Chou, J.-L.10
Drumm, M.L.11
Iannuzzi, M.C.12
Collins, F.S.13
Tsui, L.-C.14
-
4
-
-
0024453308
-
Identification of the cystic fibrosis gene: Chromosome walking and jumping
-
Rommens, J.M., Iannuzzi, M.C., Kerem, B.-S., Drumm, M.L., Melmer, G., Dean, M., Rozmahel, R., Cole, J.L., Kennedy, D., Hidaka, N., Zsiga, M., Buchwald, M., Riordan, J.R., Tsui, L.-C and Collins, F.S. (1989) Identification of the cystic fibrosis gene: chromosome walking and jumping. Science. 245, 1059-1065.
-
(1989)
Science
, vol.245
, pp. 1059-1065
-
-
Rommens, J.M.1
Iannuzzi, M.C.2
Kerem, B.-S.3
Drumm, M.L.4
Melmer, G.5
Dean, M.6
Rozmahel, R.7
Cole, J.L.8
Kennedy, D.9
Hidaka, N.10
Zsiga, M.11
Buchwald, M.12
Riordan, J.R.13
Tsui, L.-C.14
Collins, F.S.15
-
5
-
-
0027399222
-
Sickly channels in mild disease
-
Miller, C. (1993) Sickly channels in mild disease. Nature, 362, 106.
-
(1993)
Nature
, vol.362
, pp. 106
-
-
Miller, C.1
-
6
-
-
0000026508
-
Cystic fibrosis
-
Scriver, C.R., Beaudet A.L., Sly, W.S. and Valle, D. (eds), McGraw-Hill. New York, NY
-
Welsh, M.J., Tsui, L.-C., Boat, T.F. and Beaudet A.L. (1995) Cystic fibrosis. In Scriver, C.R., Beaudet A.L., Sly, W.S. and Valle, D. (eds), The Metabolic and Molecular Bases of Inherited Disease, 7th edn. McGraw-Hill. New York, NY, Vol. 3, pp. 3799-3876.
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease, 7th Edn.
, vol.3
, pp. 3799-3876
-
-
Welsh, M.J.1
Tsui, L.-C.2
Boat, T.F.3
Beaudet, A.L.4
-
7
-
-
0014411090
-
Reproductive failure in males with cystic fibrosis
-
Kaplan, E., Schwachman, H., Perlmuter, A.D., Rule, A., Khaw, K.-T. and Holsclaw, D.S. (1968) Reproductive failure in males with cystic fibrosis. N. Engl. J. Med., 279, 65-69.
-
(1968)
N. Engl. J. Med.
, vol.279
, pp. 65-69
-
-
Kaplan, E.1
Schwachman, H.2
Perlmuter, A.D.3
Rule, A.4
Khaw, K.-T.5
Holsclaw, D.S.6
-
8
-
-
0014638684
-
Abnormality of the epididymis and vas deferens in cystic fibrosis
-
Landing, B.H., Wells, T.R. and Wang, C.-I. (1969) Abnormality of the epididymis and vas deferens in cystic fibrosis, Arch. Pathol., 88, 569-580.
-
(1969)
Arch. Pathol.
, vol.88
, pp. 569-580
-
-
Landing, B.H.1
Wells, T.R.2
Wang, C.-I.3
-
9
-
-
0025763420
-
A fertile male with cystic fibrosis: Molecular genetic analysis
-
Barreto, C., Pinto, L.M., Duarte, A., Lavinha, J. and Ramsay, M. (1991) A fertile male with cystic fibrosis: molecular genetic analysis. J. Med. Genet., 28, 420-421.
-
(1991)
J. Med. Genet.
, vol.28
, pp. 420-421
-
-
Barreto, C.1
Pinto, L.M.2
Duarte, A.3
Lavinha, J.4
Ramsay, M.5
-
10
-
-
0026562867
-
Congenital bilateral absence of the vas deferens: A primarily genital form of cystic fibrosis
-
Anguiano, A., Oates, R.D., Amos, J.A., Dean, M., Gerrard, B., Steward, C., Maher, T.A. and White, M.B. (1992) Congenital bilateral absence of the vas deferens: a primarily genital form of cystic fibrosis. J. Am. Med. Assoc., 267, 1794-1797.
-
(1992)
J. Am. Med. Assoc.
, vol.267
, pp. 1794-1797
-
-
Anguiano, A.1
Oates, R.D.2
Amos, J.A.3
Dean, M.4
Gerrard, B.5
Steward, C.6
Maher, T.A.7
White, M.B.8
-
11
-
-
0027438374
-
Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens
-
Osborne, L.R., Lynch, M., Middleton, P.G., Alton, E.W.F.W., Geddes, D.M., Pryor, J.R., Hodson, M.E. and Santis, G.K. (1993) Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens. Hum. Mol. Genet., 2, 1605-1609.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1605-1609
-
-
Osborne, L.R.1
Lynch, M.2
Middleton, P.G.3
Alton, E.W.F.W.4
Geddes, D.M.5
Pryor, J.R.6
Hodson, M.E.7
Santis, G.K.8
-
12
-
-
0028281799
-
Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens
-
Culard, J.F., Desgeorges, M., Costa, P., Laussel, M., Razakatzara, G., Navratil, H., Demaille, J. and Claustres, M. (1994) Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens. Hum. Genet., 93, 467-470.
-
(1994)
Hum. Genet.
, vol.93
, pp. 467-470
-
-
Culard, J.F.1
Desgeorges, M.2
Costa, P.3
Laussel, M.4
Razakatzara, G.5
Navratil, H.6
Demaille, J.7
Claustres, M.8
-
13
-
-
0028069337
-
The genetic basis of congenital absence of the vas deferens and cystic fibrosis
-
Oates, R.D. and Amos, J.A. (1994) The genetic basis of congenital absence of the vas deferens and cystic fibrosis. J. Androl., 15, 1-8.
-
(1994)
J. Androl.
, vol.15
, pp. 1-8
-
-
Oates, R.D.1
Amos, J.A.2
-
14
-
-
0028878970
-
Extensive analysis of 40 infertile patients with congenital absence of vas deferens: In 50% of cases only one CFTR allele could be detected
-
Casals, T., Bassas, LI., Ruiz-Romero, J., Chillón, M., Gimenez, J., Ramos, M.D., Tapia, G., Narváez, H., Nunes, V. and Estivill, X. (1995) Extensive analysis of 40 infertile patients with congenital absence of vas deferens: in 50% of cases only one CFTR allele could be detected. Hum. Genet., 95, 205-211.
-
(1995)
Hum. Genet.
, vol.95
, pp. 205-211
-
-
Casals, T.1
Bassas, L.I.2
Ruiz-Romero, J.3
Chillón, M.4
Gimenez, J.5
Ramos, M.D.6
Tapia, G.7
Narváez, H.8
Nunes, V.9
Estivill, X.10
-
15
-
-
0029025333
-
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens
-
Chillón, M., Casals, T., Mercier, B., Bassas, LI., Lissens, W., Silber, S., Romey, M.C., Ruiz-Romero, J., Verlingue, C., Claustres, M., Nunes, V., Férec, C. and Estivill, X. (1995) Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N. Engl. J. Med., 332, 1475-1480.
-
(1995)
N. Engl. J. Med.
, vol.332
, pp. 1475-1480
-
-
Chillón, M.1
Casals, T.2
Mercier, B.3
Bassas, L.I.4
Lissens, W.5
Silber, S.6
Romey, M.C.7
Ruiz-Romero, J.8
Verlingue, C.9
Claustres, M.10
Nunes, V.11
Férec, C.12
Estivill, X.13
-
16
-
-
0028791190
-
n 5T allele in men with congenital bilateral absence of vas deferens
-
n 5T allele in men with congenital bilateral absence of vas deferens. Eur. J. Hum. Genet., 3, 285-293.
-
(1995)
Eur. J. Hum. Genet.
, vol.3
, pp. 285-293
-
-
Costes, B.1
Girodon, E.2
Ghanem, N.3
Flori, E.4
Jardin, A.5
Soufir, J.C.6
Goossens, M.7
-
17
-
-
0029019461
-
Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia
-
Jarvi, K., Zielenski, J., Wilschanski, M., Durie, P., Buckspan, M., Tullis, E., Markievicz, D. and Tsui, L.-C. (1995) Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia. Lancet, 345, 1578.
-
(1995)
Lancet
, vol.345
, pp. 1578
-
-
Jarvi, K.1
Zielenski, J.2
Wilschanski, M.3
Durie, P.4
Buckspan, M.5
Tullis, E.6
Markievicz, D.7
Tsui, L.-C.8
-
18
-
-
0028794627
-
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients
-
Mercier, B., Verlingue, C., Lissens, W., Silber, S.J., Novelli, G., Bonduelle, M., Audrézet, M.P. and Férec, C. (1995) Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients. Am. J. Hum. Genet., 56, 272-277.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 272-277
-
-
Mercier, B.1
Verlingue, C.2
Lissens, W.3
Silber, S.J.4
Novelli, G.5
Bonduelle, M.6
Audrézet, M.P.7
Férec, C.8
-
19
-
-
0029057474
-
CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens
-
Rave-Harel, N., Madgar, I., Goshen, R., Nissim-Rafinia, M., Ziadni, A., Rahat, A., Chiba, O., Kaiman, Y.M., Brautbar, C., Levinson, D., Augarten, A., Kerem, E. and Kerem, B. (1995) CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens. Am. J. Hum. Genet., 56, 1359-1366.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1359-1366
-
-
Rave-Harel, N.1
Madgar, I.2
Goshen, R.3
Nissim-Rafinia, M.4
Ziadni, A.5
Rahat, A.6
Chiba, O.7
Kaiman, Y.M.8
Brautbar, C.9
Levinson, D.10
Augarten, A.11
Kerem, E.12
Kerem, B.13
-
20
-
-
1842339924
-
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens
-
Dörk, T., Dworniczak, B., Aulehla-Scholz, C., Wieczorek, D., Böhm, I., Mayerova, A., Seydewitz, H.H., Nieschlag, E., Meschede, D., Horst, J., Pander, H.-J., Sperling, H., Ratjen, F., Passarge, E., Schmidtke, J. and Stuhrmann, M. (1997) Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens. Hum. Genet., 100, 365-377.
-
(1997)
Hum. Genet.
, vol.100
, pp. 365-377
-
-
Dörk, T.1
Dworniczak, B.2
Aulehla-Scholz, C.3
Wieczorek, D.4
Böhm, I.5
Mayerova, A.6
Seydewitz, H.H.7
Nieschlag, E.8
Meschede, D.9
Horst, J.10
Pander, H.-J.11
Sperling, H.12
Ratjen, F.13
Passarge, E.14
Schmidtke, J.15
Stuhrmann, M.16
-
21
-
-
0025906695
-
Variable delection of exon 9 coding sequences in cystic fibrosis transmembrane conductance regulator gene mRNA transcripts in normal bronchial epithelium
-
Chu, C.S., Trapnell, B.C., Murtagh, J.J. Jr. Moss, J., Dalemans, W., Jallat, S., Mercenier, A., Pavirani, A., Lecocq, J.P., Cutting, G.R., Guggino, W.B. and Crystal, R.G. (1991) Variable delection of exon 9 coding sequences in cystic fibrosis transmembrane conductance regulator gene mRNA transcripts in normal bronchial epithelium. EMBO J., 10, 1355-1363.
-
(1991)
EMBO J.
, vol.10
, pp. 1355-1363
-
-
Chu, C.S.1
Trapnell, B.C.2
Murtagh Jr., J.J.3
Moss, J.4
Dalemans, W.5
Jallat, S.6
Mercenier, A.7
Pavirani, A.8
Lecocq, J.P.9
Cutting, G.R.10
Guggino, W.B.11
Crystal, R.G.12
-
22
-
-
0027502580
-
Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA
-
Chu, C.S., Trapnell, B.C., Curristin, S., Cutting, G.R. and Crystal, R.G. (1993) Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA. Nature Genet., 3, 151-156.
-
(1993)
Nature Genet.
, vol.3
, pp. 151-156
-
-
Chu, C.S.1
Trapnell, B.C.2
Curristin, S.3
Cutting, G.R.4
Crystal, R.G.5
-
23
-
-
0031023970
-
Increased proportion of exon 9 alternatively spliced CFTR transcripts in vas deferens compared with nasal epithelial cells
-
Teng, H., Jorissen, M., Poppel, H., Legius, E., Cassiman, J.J. and Cuppens, H. (1997) Increased proportion of exon 9 alternatively spliced CFTR transcripts in vas deferens compared with nasal epithelial cells. Hum. Mol. Genet., 6, 85-90.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 85-90
-
-
Teng, H.1
Jorissen, M.2
Poppel, H.3
Legius, E.4
Cassiman, J.J.5
Cuppens, H.6
-
24
-
-
0030687683
-
Higher proportion of intact exon 9 mRNA in nasal epithelium compared with vas deferens
-
Mak, V., Jarvi, K.A., Zielenski, J., Durie, P. and Tsui, L.-C. (1997) Higher proportion of intact exon 9 mRNA in nasal epithelium compared with vas deferens. Hum. Mol. Genet., 6, 2099-2107.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2099-2107
-
-
Mak, V.1
Jarvi, K.A.2
Zielenski, J.3
Durie, P.4
Tsui, L.-C.5
-
25
-
-
0031037337
-
The molecular basis of partial penetrance of splicing mutations in cystic fibrosis
-
Rave-Harel, N., Kerem, E., Nissim-Rafinia, M., Madjar, I., Goshen, R., Augarten, A., Rahat, A., Hurwitz, A., Darvasi, A. and Kerem, B. (1997) The molecular basis of partial penetrance of splicing mutations in cystic fibrosis. Am. J. Hum. Genet., 60, 87-94.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 87-94
-
-
Rave-Harel, N.1
Kerem, E.2
Nissim-Rafinia, M.3
Madjar, I.4
Goshen, R.5
Augarten, A.6
Rahat, A.7
Hurwitz, A.8
Darvasi, A.9
Kerem, B.10
-
26
-
-
0025947566
-
The fertility potential of male cystic fibrosis patients
-
Gottlieb, C., Ploen, L., Kvist, U. and Standvik, B. (1991) The fertility potential of male cystic fibrosis patients. Int. J. Androl., 14, 437-440.
-
(1991)
Int. J. Androl.
, vol.14
, pp. 437-440
-
-
Gottlieb, C.1
Ploen, L.2
Kvist, U.3
Standvik, B.4
-
27
-
-
0028069337
-
The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis
-
Oates, R.D. and Amos, J.A. (1994) The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis. J. Androl., 15, 1-8.
-
(1994)
J. Androl.
, vol.15
, pp. 1-8
-
-
Oates, R.D.1
Amos, J.A.2
-
28
-
-
0031433107
-
High heterogeneity for cystic fibrosis in Spanish families: 75 mutations account for 90% of chromosomes
-
Casals, T., Ramos, M.D., Giménez, J., Larriba, S., Nunes, V. and Estivill, X. (1997) High heterogeneity for cystic fibrosis in Spanish families: 75 mutations account for 90% of chromosomes. Hum. Genet., 101, 365-370.
-
(1997)
Hum. Genet.
, vol.101
, pp. 365-370
-
-
Casals, T.1
Ramos, M.D.2
Giménez, J.3
Larriba, S.4
Nunes, V.5
Estivill, X.6
-
29
-
-
0029883545
-
Cystic fibrosis mutation screening in healthy men with reduced sperm quality
-
van der Ven, K., Messer, L., van der Ven, H., Jeyendran, R.S. and Ober, C. (1996) Cystic fibrosis mutation screening in healthy men with reduced sperm quality. Hum. Reprod., 11, 513-517.
-
(1996)
Hum. Reprod.
, vol.11
, pp. 513-517
-
-
Van Der Ven, K.1
Messer, L.2
Van Der Ven, H.3
Jeyendran, R.S.4
Ober, C.5
-
30
-
-
0029151485
-
CFTR gene variant for patients with congenital absence of vas deferens
-
Zielenski, J., Patrizio, P., Corey, M., Handelin, B., Markiewicz, D., Asch, R. and Tsui, L.-C. (1995) CFTR gene variant for patients with congenital absence of vas deferens. Am. J. Hum. Genet., 57, 958-960.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 958-960
-
-
Zielenski, J.1
Patrizio, P.2
Corey, M.3
Handelin, B.4
Markiewicz, D.5
Asch, R.6
Tsui, L.-C.7
-
31
-
-
1842339924
-
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens
-
Dörk, T., Dworniczak, B., Aulehla-Scholz, C., Wieczorek, D., Böhm, I., Mayerova, A., Seydewitz, H., Nieschlag, E., Meschede, D., Horst, J., Pander, H.-J., Sperling, H., Ratjen, F., Passarge, E., Schmidtke, J. and Sturhrmann, M. (1997) Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens. Hum. Genet., 100, 365-377.
-
(1997)
Hum. Genet.
, vol.100
, pp. 365-377
-
-
Dörk, T.1
Dworniczak, B.2
Aulehla-Scholz, C.3
Wieczorek, D.4
Böhm, I.5
Mayerova, A.6
Seydewitz, H.7
Nieschlag, E.8
Meschede, D.9
Horst, J.10
Pander, H.-J.11
Sperling, H.12
Ratjen, F.13
Passarge, E.14
Schmidtke, J.15
Sturhrmann, M.16
-
32
-
-
0027310434
-
Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance
-
Strong, T.V., Wilkinson, D.J., Mansoura, M.K., Devor, D.C., Henze, K., Yang, Y., Wilson, J.M., Cohn, J.A., Dawson, D.C., Frizzell, R.A. and Collins, F.S. (1993) Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance. Hum. Mol. Genet., 2, 225-230.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 225-230
-
-
Strong, T.V.1
Wilkinson, D.J.2
Mansoura, M.K.3
Devor, D.C.4
Henze, K.5
Yang, Y.6
Wilson, J.M.7
Cohn, J.A.8
Dawson, D.C.9
Frizzell, R.A.10
Collins, F.S.11
-
33
-
-
0023230443
-
Correlation between spermatozoon numbers in spermiogram and seminiferous epithelium histology in testicular biopsies from subfertile men
-
Nistal, M., Codesal, J., Santamaría, L. and Paniagua, R. (1987) Correlation between spermatozoon numbers in spermiogram and seminiferous epithelium histology in testicular biopsies from subfertile men. Fertil. Steril., 48, 507-509.
-
(1987)
Fertil. Steril.
, vol.48
, pp. 507-509
-
-
Nistal, M.1
Codesal, J.2
Santamaría, L.3
Paniagua, R.4
-
34
-
-
0019423473
-
Quantitative analysis of testicle biopsy: Determination of partial obstruction and prediction of sperm count after surgery for obstruction
-
Silber, S.J. and Rodriguez-Rigau, L.J. (1981) Quantitative analysis of testicle biopsy: determination of partial obstruction and prediction of sperm count after surgery for obstruction. Fertil. Steril., 36, 480-485.
-
(1981)
Fertil. Steril.
, vol.36
, pp. 480-485
-
-
Silber, S.J.1
Rodriguez-Rigau, L.J.2
-
35
-
-
0025787393
-
In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator
-
Trezise, A.E.O. and Buchwald, M. (1991) In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator. Nature, 353, 434-437.
-
(1991)
Nature
, vol.353
, pp. 434-437
-
-
Trezise, A.E.O.1
Buchwald, M.2
-
36
-
-
0027450848
-
CFTR expression is regulated during both the cycle of the seminiferous epithelium and the oestrus cycle of rodents
-
Trezise, A.E.O., Linder, C.C., Grieger, D., Thompson, E.W., Meunier, H., Griswold, M.D. and Buchwald, M. (1993) CFTR expression is regulated during both the cycle of the seminiferous epithelium and the oestrus cycle of rodents. Nature Genet., 3, 157-164.
-
(1993)
Nature Genet.
, vol.3
, pp. 157-164
-
-
Trezise, A.E.O.1
Linder, C.C.2
Grieger, D.3
Thompson, E.W.4
Meunier, H.5
Griswold, M.D.6
Buchwald, M.7
-
37
-
-
0027172086
-
Cystic fibrosis mutations impair the fertilization rate of epididymal sperm from men with congenital absence of vas deferens
-
Patrizio, P., Ord, T, Silber, S.J. and Asch, R.H. (1993) Cystic fibrosis mutations impair the fertilization rate of epididymal sperm from men with congenital absence of vas deferens. Hum. Reprod., 8, 1259-1263.
-
(1993)
Hum. Reprod.
, vol.8
, pp. 1259-1263
-
-
Patrizio, P.1
Ord, T.2
Silber, S.J.3
Asch, R.H.4
-
38
-
-
1842353216
-
Analysis of human chromosome specific reiterated DNA in chromosome variants
-
Kunkel, L.M., Smith, K.D., Boyer, S.H., Borgaonkar, D.S., Watchel, S.S., Miller, O.J., Breg, W.R., Jone, H.W. and Rary, J.M. (1977) Analysis of human chromosome specific reiterated DNA in chromosome variants. Proc. Natl Acad. Sci. USA, 74, 1245-1249.
-
(1977)
Proc. Natl Acad. Sci. USA
, vol.74
, pp. 1245-1249
-
-
Kunkel, L.M.1
Smith, K.D.2
Boyer, S.H.3
Borgaonkar, D.S.4
Watchel, S.S.5
Miller, O.J.6
Breg, W.R.7
Jone, H.W.8
Rary, J.M.9
|