-
1
-
-
0024256103
-
Epileptic syndromes in childhood
-
Aicardi, J. (1988). Epileptic syndromes in childhood. Epilepsia 29, S1-S5.
-
(1988)
Epilepsia
, vol.29
-
-
Aicardi, J.1
-
2
-
-
0000476788
-
Die gruppierung der epilepsie
-
Alzheimer, A. (1907). Die Gruppierung der Epilepsie. Allg. Z. Psychiatrie 64, 418-421.
-
(1907)
Allg. Z. Psychiatrie
, vol.64
, pp. 418-421
-
-
Alzheimer, A.1
-
3
-
-
0026567180
-
Gray matter heterotopias: MR characteristics and correlation with developmental and neurological manifestations
-
Barkovich, A.J., and Kjos, B. (1992). Gray matter heterotopias: MR characteristics and correlation with developmental and neurological manifestations. Radiology 182, 483-499.
-
(1992)
Radiology
, vol.182
, pp. 483-499
-
-
Barkovich, A.J.1
Kjos, B.2
-
4
-
-
0027967042
-
X-linked pachygyria and agenesis of the corpus callosum: Evidence for an X chromosome lissencephaly locus
-
Berry-Kravis, E., and Israel, J. (1994). X-linked pachygyria and agenesis of the corpus callosum: evidence for an X chromosome lissencephaly locus. Ann. Neurol. 36, 229-233.
-
(1994)
Ann. Neurol.
, vol.36
, pp. 229-233
-
-
Berry-Kravis, E.1
Israel, J.2
-
5
-
-
0027524597
-
Transcriptional organization of a 450-kb region of the human X chromosome in Xq28
-
Bione, S., Tamanini, F., Maestrini, E., Tribioli, C., Poustka, A., Torri, G., Rivella, S., and Toniolo, D. (1993). Transcriptional organization of a 450-kb region of the human X chromosome in Xq28. Proc. Natl. Acad. Sci. USA 90, 10977-10981.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 10977-10981
-
-
Bione, S.1
Tamanini, F.2
Maestrini, E.3
Tribioli, C.4
Poustka, A.5
Torri, G.6
Rivella, S.7
Toniolo, D.8
-
6
-
-
0028082058
-
Progress in mapping human epilepsy genes
-
Delgado-Escueta, A.V., Serratosa, J.M., Liu, A., Weissbecker, K., Medina, M.T., Gee, M., Treiman, L.J., and Sparkes, R.S. (1994). Progress in mapping human epilepsy genes. Epilepsia 35 (Suppl.), S29-S40.
-
(1994)
Epilepsia
, vol.35
, Issue.SUPPL.
-
-
Delgado-Escueta, A.V.1
Serratosa, J.M.2
Liu, A.3
Weissbecker, K.4
Medina, M.T.5
Gee, M.6
Treiman, L.J.7
Sparkes, R.S.8
-
7
-
-
0027312620
-
Familial band heterotopias simulating tuberous sclerosis
-
DiMario, F.J., Cobb, R.J., Ramsby, G.R., and Leicher, C. (1993). Familial band heterotopias simulating tuberous sclerosis. Neurology 43, 1424-1426.
-
(1993)
Neurology
, vol.43
, pp. 1424-1426
-
-
DiMario, F.J.1
Cobb, R.J.2
Ramsby, G.R.3
Leicher, C.4
-
8
-
-
0026780723
-
Causal heterogeneity in isolated lissencephaly
-
Dobyns, W.B., Elias, E.R., Newlin, A.C., Pagon, R.A., and Ledbetter, D.H. (1992). Causal heterogeneity in isolated lissencephaly. Neurology 42, 1375-1388.
-
(1992)
Neurology
, vol.42
, pp. 1375-1388
-
-
Dobyns, W.B.1
Elias, E.R.2
Newlin, A.C.3
Pagon, R.A.4
Ledbetter, D.H.5
-
9
-
-
0028264926
-
A linkage map of microsatellite markers on the human X chromosome
-
Donnelly, A., Kozman, H., Gedeon, A.K., Webb, S., Lynch, M., Sutherland, G.R., Richards, R.I., and Mulley, J.C. (1994). A linkage map of microsatellite markers on the human X chromosome. Genomics 20, 363-370.
-
(1994)
Genomics
, vol.20
, pp. 363-370
-
-
Donnelly, A.1
Kozman, H.2
Gedeon, A.K.3
Webb, S.4
Lynch, M.5
Sutherland, G.R.6
Richards, R.I.7
Mulley, J.C.8
-
10
-
-
0027770784
-
Identification and characterization of the tuberous sclerosis gene on chromosome 16
-
The European Chromosome 16 Tuberous Sclerosis Consortium (1993). Identification and characterization of the tuberous sclerosis gene on chromosome 16. Cell 75, 1305-1315.
-
(1993)
Cell
, vol.75
, pp. 1305-1315
-
-
-
11
-
-
0028895748
-
A 2D crossover-based map of the human X chromosome as a model for map integration
-
Fain, P.R., Kort, E.N., Chance, P.F., Nguyen, K., Redd, D.F., Econs, M.J., and Barker, D.P. (1995). A 2D crossover-based map of the human X chromosome as a model for map integration. Nature Genet. 9, 261-266.
-
(1995)
Nature Genet.
, vol.9
, pp. 261-266
-
-
Fain, P.R.1
Kort, E.N.2
Chance, P.F.3
Nguyen, K.4
Redd, D.F.5
Econs, M.J.6
Barker, D.P.7
-
12
-
-
0026540749
-
Neuropathologic findings in cortical resections (including hemispherectomies) performed for the treatment of intractable childhood epilepsy
-
Farrell, M.A., DeRosa, M.J., Curran, J.G., Lenard Secor, D., Cornford, M.E., Comair, Y.G., Peacock, W.J., Shields, W.D., and Vinters, H.V. (1992). Neuropathologic findings in cortical resections (including hemispherectomies) performed for the treatment of intractable childhood epilepsy. Acta Neuropathologica 83, 246-259.
-
(1992)
Acta Neuropathologica
, vol.83
, pp. 246-259
-
-
Farrell, M.A.1
DeRosa, M.J.2
Curran, J.G.3
Lenard Secor, D.4
Cornford, M.E.5
Comair, Y.G.6
Peacock, W.J.7
Shields, W.D.8
Vinters, H.V.9
-
13
-
-
0028170112
-
The GDB™ Human Genome Data Base anno 1994
-
Fasman, K.H., Cuticchia, A.J., and Kingsbury, D.T. (1994). The GDB™ Human Genome Data Base anno 1994. Nucl. Acids Res. 22, 3462-3469.
-
(1994)
Nucl. Acids Res.
, vol.22
, pp. 3462-3469
-
-
Fasman, K.H.1
Cuticchia, A.J.2
Kingsbury, D.T.3
-
14
-
-
0027089750
-
Identification of a second pseudo-autosomal region near the Xq and Yq telomeres
-
Freije, D., Helms, C., Watson, M.S., and Donis-Keller, H. (1992). Identification of a second pseudo-autosomal region near the Xq and Yq telomeres. Science 258, 1784-1787.
-
(1992)
Science
, vol.258
, pp. 1784-1787
-
-
Freije, D.1
Helms, C.2
Watson, M.S.3
Donis-Keller, H.4
-
16
-
-
0023712810
-
Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci in human chromosome 6
-
Greenberg, D.A., Delgado-Escueta, A.V., Widelitz, H., Sparkes, R.S., Treiman, L., Maldonado, H.M., Park, M.S., and Terasaki, P.I. (1988). Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci in human chromosome 6. Am. J. Med. Genet. 31, 185-192.
-
(1988)
Am. J. Med. Genet.
, vol.31
, pp. 185-192
-
-
Greenberg, D.A.1
Delgado-Escueta, A.V.2
Widelitz, H.3
Sparkes, R.S.4
Treiman, L.5
Maldonado, H.M.6
Park, M.S.7
Terasaki, P.I.8
-
17
-
-
0028231090
-
The 1993-94 Généthon human genetic linkage map
-
Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. (1994). The 1993-94 Généthon human genetic linkage map. Nature Genet. 7, 246-339.
-
(1994)
Nature Genet.
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
18
-
-
0023694274
-
Microdysgenesis in resected temporal neocortex: Incidence and clinical significance in focal epilepsy
-
Hardiman, O., Burke, T., Phillips, J., Murphy, S., O'Moore, B., Staunton, H., and Farrell, M.A. (1988). Microdysgenesis in resected temporal neocortex: incidence and clinical significance in focal epilepsy. Neurology 38, 1041-1047.
-
(1988)
Neurology
, vol.38
, pp. 1041-1047
-
-
Hardiman, O.1
Burke, T.2
Phillips, J.3
Murphy, S.4
O'Moore, B.5
Staunton, H.6
Farrell, M.A.7
-
19
-
-
0028023599
-
Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor
-
Hattori, M., Adachl, H., Trujimoto, M., Arai, H., and Inoue, K. (1994). Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor. Nature 370, 216-218.
-
(1994)
Nature
, vol.370
, pp. 216-218
-
-
Hattori, M.1
Adachl, H.2
Trujimoto, M.3
Arai, H.4
Inoue, K.5
-
21
-
-
0342919697
-
Familial periventricular heterotopias and seizures in four generations
-
Huttenlocher, P.R., Taravath, S., and Mojtahedi, S. (1991). Familial periventricular heterotopias and seizures in four generations. Ann. Neurol. 30, 461.
-
(1991)
Ann. Neurol.
, vol.30
, pp. 461
-
-
Huttenlocher, P.R.1
Taravath, S.2
Mojtahedi, S.3
-
22
-
-
0028157014
-
Periventricular heterotopias and epilepsy
-
Huttenlocher, P.R., Taravath, S., and Mojtahedi, M. (1994). Periventricular heterotopias and epilepsy. Neurology 44, 51-55.
-
(1994)
Neurology
, vol.44
, pp. 51-55
-
-
Huttenlocher, P.R.1
Taravath, S.2
Mojtahedi, M.3
-
23
-
-
0028241952
-
X-linked spastic paraplegia (SPG-1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene
-
Jouet, M., Rosenthal, A., Armstrong, G., MacFarlane, J., Stevenson, R., Paterson, J., Metzenberg, A., Ionasescu, V., Temple, K., and Kenwick, S. (1994). X-linked spastic paraplegia (SPG-1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene. Nature Genet. 7, 402-407.
-
(1994)
Nature Genet.
, vol.7
, pp. 402-407
-
-
Jouet, M.1
Rosenthal, A.2
Armstrong, G.3
MacFarlane, J.4
Stevenson, R.5
Paterson, J.6
Metzenberg, A.7
Ionasescu, V.8
Temple, K.9
Kenwick, S.10
-
24
-
-
0027215439
-
Familial periventricular nodular heterotopia
-
Kamuro, K., and Tenokuchi, Y. (1993). Familial periventricular nodular heterotopia. Brain Dev. 15, 237-241.
-
(1993)
Brain Dev.
, vol.15
, pp. 237-241
-
-
Kamuro, K.1
Tenokuchi, Y.2
-
25
-
-
0029122621
-
Radial and horizontal deployment of clonally related cells in the primate neocortex: Relationship to distinct mitotic lineages
-
Kornack, D.R., and Rakic, P. (1995). Radial and horizontal deployment of clonally related cells in the primate neocortex: relationship to distinct mitotic lineages. Neuron 15, 311-321.
-
(1995)
Neuron
, vol.15
, pp. 311-321
-
-
Kornack, D.R.1
Rakic, P.2
-
26
-
-
0025822844
-
Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene
-
Lalloz, M.R.A., McVey, J.H., Pattinson, J.K., and Tuddenham, E.G.D. (1991). Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene. Lancet 338, 207-211.
-
(1991)
Lancet
, vol.338
, pp. 207-211
-
-
Lalloz, M.R.A.1
McVey, J.H.2
Pattinson, J.K.3
Tuddenham, E.G.D.4
-
27
-
-
0021344005
-
Easy calculations of lod scores and genetic risks on small computers
-
Lathrop, G.M., and Lalouel, J.M. (1984). Easy calculations of lod scores and genetic risks on small computers. Am. J. Hum. Genet. 36, 460-465.
-
(1984)
Am. J. Hum. Genet.
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
28
-
-
0023933932
-
Efficient computations in multilocus linkage analysis
-
Lathrop, G.M., and Lalouel, J.M. (1988). Efficient computations in multilocus linkage analysis. Am. J. Hum. Genet. 42, 498-505.
-
(1988)
Am. J. Hum. Genet.
, vol.42
, pp. 498-505
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
29
-
-
0021046979
-
L1 mono- and polyclonal antibodies modify cell migration in early postnatal mouse cerebellum
-
Lindner, J., Rathjen, F., and Schachner, M. (1983). L1 mono- and polyclonal antibodies modify cell migration in early postnatal mouse cerebellum. Nature 305, 427-429.
-
(1983)
Nature
, vol.305
, pp. 427-429
-
-
Lindner, J.1
Rathjen, F.2
Schachner, M.3
-
30
-
-
0027183463
-
Shadow bands seen when typing polymorphic dinucleotide repeats: Some causes and cures
-
Litt, M., Hauge, X., and Sharma, V. (1993). Shadow bands seen when typing polymorphic dinucleotide repeats: some causes and cures. Biotechniques 15, 280-284.
-
(1993)
Biotechniques
, vol.15
, pp. 280-284
-
-
Litt, M.1
Hauge, X.2
Sharma, V.3
-
31
-
-
0027410493
-
Neurons, astrocytes, and oligodendrocytes of the rat cerebral cortex originate from separate progenitor cells: An ultrastructural analysis of clonally related cells
-
Luskin, M.B., Parnavelas, J.G., and Barfield, J.A. (1993). Neurons, astrocytes, and oligodendrocytes of the rat cerebral cortex originate from separate progenitor cells: an ultrastructural analysis of clonally related cells. J. Neurosci. 13, 1730-1750.
-
(1993)
J. Neurosci.
, vol.13
, pp. 1730-1750
-
-
Luskin, M.B.1
Parnavelas, J.G.2
Barfield, J.A.3
-
32
-
-
0021368047
-
Neuropathological findings in primary generalized epilepsy: A study of eight cases
-
Meencke, H.J., and Janz, D. (1984). Neuropathological findings in primary generalized epilepsy: a study of eight cases. Epilepsia 25, 8-21.
-
(1984)
Epilepsia
, vol.25
, pp. 8-21
-
-
Meencke, H.J.1
Janz, D.2
-
33
-
-
0027338402
-
A receptor subunit genes is deleted in a neurological mutant of the mouse p locus
-
A receptor subunit genes is deleted in a neurological mutant of the mouse p locus. Nature 364, 448-450.
-
(1993)
Nature
, vol.364
, pp. 448-450
-
-
Nakatsu, Y.1
Tyndale, R.F.2
DeLorey, T.M.3
Durham-Pierre, D.4
Gardner, J.M.5
McDanel, H.J.6
Nguyen, Q.7
Wagstaff, J.8
Lalande, M.9
Sikela, J.M.10
-
34
-
-
0027257653
-
Hereditary nodular heterotopia accompanied by mega cisterna magna
-
Oda, T., Nagai, Y., Fuijimoto, S., Sobajima, H., Kobayashi, M., Togari, H., and Wada, Y. (1993). Hereditary nodular heterotopia accompanied by mega cisterna magna. Am. J. Med. Genet. 47, 268-271.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 268-271
-
-
Oda, T.1
Nagai, Y.2
Fuijimoto, S.3
Sobajima, H.4
Kobayashi, M.5
Togari, H.6
Wada, Y.7
-
35
-
-
0029059069
-
Localization of a gene for partial epilepsy to chromosome 10q
-
Ottman, R., Risch, N., Hauser, W.A., Pedley, T.A., Lee, J.H., Barker-Cummings, C., Lustenberger, A., Nagle, K.J., Lee, K.S., et al. (1995). Localization of a gene for partial epilepsy to chromosome 10q. Nature Genet. 10, 56-60.
-
(1995)
Nature Genet.
, vol.10
, pp. 56-60
-
-
Ottman, R.1
Risch, N.2
Hauser, W.A.3
Pedley, T.A.4
Lee, J.H.5
Barker-Cummings, C.6
Lustenberger, A.7
Nagle, K.J.8
Lee, K.S.9
-
36
-
-
0026253198
-
Separate progenitor cells give rise to pyramidal and nonpyramidal neurons in the rat telencephalon
-
Parnavelas, J.G., Barfield, J.A., Franke, E., and Luskin, M.B. (1991). Separate progenitor cells give rise to pyramidal and nonpyramidal neurons in the rat telencephalon. Cereb. Cortex 1, 463-468.
-
(1991)
Cereb. Cortex
, vol.1
, pp. 463-468
-
-
Parnavelas, J.G.1
Barfield, J.A.2
Franke, E.3
Luskin, M.B.4
-
37
-
-
0029045967
-
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2
-
Phillips, H.A., Scheffer, I.E., Berkovic, S.F., Holloway, G.E., Sutherland, G.R., and Mulley, J.C. (1995). Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2. Nature Genet. 10, 117-118.
-
(1995)
Nature Genet.
, vol.10
, pp. 117-118
-
-
Phillips, H.A.1
Scheffer, I.E.2
Berkovic, S.F.3
Holloway, G.E.4
Sutherland, G.R.5
Mulley, J.C.6
-
38
-
-
0028021189
-
Subcortical laminar heterotopia and lissencephaly in two families: A single X-linked dominant gene
-
Pinard, J.-M., Motte, J., Chiron, C., Brain, R., Andermann, E., and Dulac, O. (1994). Subcortical laminar heterotopia and lissencephaly in two families: a single X-linked dominant gene. J. Neurol. Neurosurg. Psychiatr. 57, 914-920.
-
(1994)
J. Neurol. Neurosurg. Psychiatr.
, vol.57
, pp. 914-920
-
-
Pinard, J.-M.1
Motte, J.2
Chiron, C.3
Brain, R.4
Andermann, E.5
Dulac, O.6
-
39
-
-
0028110454
-
Subependymal heterotopia: A distinct neuronal migration disorder associated with epilepsy
-
Raymond, A.A., Fish, D.R., Stevens, J.M., Sisodiya, S.M., Alsanjari, N., and Shorvon, S.D. (1994). Subependymal heterotopia: a distinct neuronal migration disorder associated with epilepsy. J. Neurol. Neurosurg. Psychiatr. 57, 1195-1202.
-
(1994)
J. Neurol. Neurosurg. Psychiatr.
, vol.57
, pp. 1195-1202
-
-
Raymond, A.A.1
Fish, D.R.2
Stevens, J.M.3
Sisodiya, S.M.4
Alsanjari, N.5
Shorvon, S.D.6
-
40
-
-
0029149713
-
Systematic widespread clonal organization in cerebral cortex
-
Reid, C.B., Liang, I., and Walsh, C. (1995). Systematic widespread clonal organization in cerebral cortex. Neuron 15, 299-310.
-
(1995)
Neuron
, vol.15
, pp. 299-310
-
-
Reid, C.B.1
Liang, I.2
Walsh, C.3
-
41
-
-
0027176708
-
Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats
-
Reiner, O., Carrozzo, R., Shen, Y., Wehnert, M., Faustinella, F., Dobyns, W.B., Caskey, C.T., and Ledbetter, D.H. (1993). Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats. Nature 364, 717-721.
-
(1993)
Nature
, vol.364
, pp. 717-721
-
-
Reiner, O.1
Carrozzo, R.2
Shen, Y.3
Wehnert, M.4
Faustinella, F.5
Dobyns, W.B.6
Caskey, C.T.7
Ledbetter, D.H.8
-
42
-
-
84970061068
-
Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus
-
Rosenthal, A., Jouet, M., and Kenwrick, S. (1992). Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus. Nature Genet. 2, 107-112.
-
(1992)
Nature Genet.
, vol.2
, pp. 107-112
-
-
Rosenthal, A.1
Jouet, M.2
Kenwrick, S.3
-
43
-
-
0029303355
-
Partial epilepsy: Chinks in the armour
-
Ryan, S.G. (1995). Partial epilepsy: chinks in the armour. Nature Genet. 10, 4-6.
-
(1995)
Nature Genet.
, vol.10
, pp. 4-6
-
-
Ryan, S.G.1
-
44
-
-
0027368589
-
Construction of a transcription map of a 300 kb region around the human G6PD locus by direct cDNA selection
-
Sedlacek, Z., Korn, B., Konecki, D.S., Siebenhaar, R., Coy, J.F., Kioschis, P., and Poustka, A. (1993). Construction of a transcription map of a 300 kb region around the human G6PD locus by direct cDNA selection. Hum. Mol. Genet. 2, 1865-1869.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1865-1869
-
-
Sedlacek, Z.1
Korn, B.2
Konecki, D.S.3
Siebenhaar, R.4
Coy, J.F.5
Kioschis, P.6
Poustka, A.7
-
45
-
-
0026063809
-
Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers
-
Sefiani, A., M'rad, R., Simard, L., Vincent, A., Julier, C., Holvoet-Vermaut, L., Heurtz, S., Dahl, N., Stalder, J.F., Peter, M.O., et al. (1991). Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers. Hum. Genet. 89, 297-299.
-
(1991)
Hum. Genet.
, vol.89
, pp. 297-299
-
-
Sefiani, A.1
M'rad, R.2
Simard, L.3
Vincent, A.4
Julier, C.5
Holvoet-Vermaut, L.6
Heurtz, S.7
Dahl, N.8
Stalder, J.F.9
Peter, M.O.10
-
47
-
-
0028241953
-
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM
-
Vits, L., Van Camp, G., Coucke, P., Fransen, E., De Boulle, K., Reyniers, E., Korn, B., Poustka, A., Wilson, G., Schrander, C., et al. (1994). MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM. Nature Genet. 7, 408-413.
-
(1994)
Nature Genet.
, vol.7
, pp. 408-413
-
-
Vits, L.1
Van Camp, G.2
Coucke, P.3
Fransen, E.4
De Boulle, K.5
Reyniers, E.6
Korn, B.7
Poustka, A.8
Wilson, G.9
Schrander, C.10
-
48
-
-
0026510716
-
Widespread dispersion of neuronal clones across functional regions of the cerebral cortex
-
Walsh, C., and Cepko, C.L. (1992). Widespread dispersion of neuronal clones across functional regions of the cerebral cortex. Science 255, 434-440.
-
(1992)
Science
, vol.255
, pp. 434-440
-
-
Walsh, C.1
Cepko, C.L.2
-
49
-
-
0027932287
-
Integration of gene maps: Chromosome X
-
Wang, L.H., Collins, A., Lawrence, S., Keats, B.J., and Morton, N.E. (1994). Integration of gene maps: chromosome X. Genomics 22, 590-604.
-
(1994)
Genomics
, vol.22
, pp. 590-604
-
-
Wang, L.H.1
Collins, A.2
Lawrence, S.3
Keats, B.J.4
Morton, N.E.5
-
50
-
-
0027166351
-
Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134
-
Wehnert, M., Reiner, O., and Caskey, T. (1993). Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134. Hum. Mol. Genet. 2, 1503.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1503
-
-
Wehnert, M.1
Reiner, O.2
Caskey, T.3
-
51
-
-
0027722233
-
A second generation linkage map of the human genome based on highly informative microsatellite loci
-
Weissenbach, J. (1993). A second generation linkage map of the human genome based on highly informative microsatellite loci. Gene 135, 275-278.
-
(1993)
Gene
, vol.135
, pp. 275-278
-
-
Weissenbach, J.1
-
52
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach, J., Gyapay, G., Dib, C., Vignal, A., Morissette, J., Millasseau, P., Vaysseix, G., and Lathrop, M. (1992). A second-generation linkage map of the human genome. Nature 359, 794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
53
-
-
0027362601
-
Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: No evidence for an epilepsy locus in the HLA region
-
Whitehouse, W.P., Rees, M., Curtis, D., Sundqvist, A., Parker, K., Chung, E., Baralle, D., and Gardiner, R.M. (1993). Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region. Am. J. Hum. Genet. 53, 652-662.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 652-662
-
-
Whitehouse, W.P.1
Rees, M.2
Curtis, D.3
Sundqvist, A.4
Parker, K.5
Chung, E.6
Baralle, D.7
Gardiner, R.M.8
-
54
-
-
0027936475
-
Report of the fifth international workshop on human X chromosome mapping 1994
-
Willard, H.F., Cremers, F., Mandel, J.-L., Monaco, A.P., Nelson, D.L., and Schlessinger, D. (1994). Report of the fifth international workshop on human X chromosome mapping 1994. Cytogenet. Cell Genet. 67, 296-358.
-
(1994)
Cytogenet. Cell Genet.
, vol.67
, pp. 296-358
-
-
Willard, H.F.1
Cremers, F.2
Mandel, J.-L.3
Monaco, A.P.4
Nelson, D.L.5
Schlessinger, D.6
-
55
-
-
0026637344
-
New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia, and pachygyria
-
Zollino, M., Mastroiacovo, P., Zampino, G., Mariotti, P., and Neri, G. (1992). New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia, and pachygyria. Am. J. Med. Genet. 43, 452-457.
-
(1992)
Am. J. Med. Genet.
, vol.43
, pp. 452-457
-
-
Zollino, M.1
Mastroiacovo, P.2
Zampino, G.3
Mariotti, P.4
Neri, G.5
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