-
1
-
-
0015336653
-
A theory of X-linkage of major intellectual traits
-
Lehrke RG. A theory of X-linkage of major intellectual traits. Am J Ment Defic 1972;76:611-19.
-
(1972)
Am J Ment Defic
, vol.76
, pp. 611-619
-
-
Lehrke, R.G.1
-
2
-
-
0025104133
-
Assignment of X-linked hydrocephalus to Xq28 by linkage analysis
-
Willems PJ, Dijkstra I, van der Auwera BJ, et al. Assignment of X-linked hydrocephalus to Xq28 by linkage analysis. Genomics 1990;8:367-70.
-
(1990)
Genomics
, vol.8
, pp. 367-370
-
-
Willems, P.J.1
Dijkstra, I.2
Van Der Auwera, B.J.3
-
3
-
-
0029890398
-
XLMR genes: Update 1996
-
Lubs HA, Chiuazzi P, Arena JF, Schwartz CE, Tranebjaerg L, Neri G. XLMR genes: update 1996. Am J Med Genet 1996;64:147-57.
-
(1996)
Am J Med Genet
, vol.64
, pp. 147-157
-
-
Lubs, H.A.1
Chiuazzi, P.2
Arena, J.F.3
Schwartz, C.E.4
Tranebjaerg, L.5
Neri, G.6
-
4
-
-
0030138905
-
Identification of a novel gene (FMR2) associated with the FRAXE CCG repeat and CpG island
-
Gu Y, Shen Y, Gibbs RA, Nelson DL. Identification of a novel gene (FMR2) associated with the FRAXE CCG repeat and CpG island. Nat Genet 1996;13:109-13.
-
(1996)
Nat Genet
, vol.13
, pp. 109-113
-
-
Gu, Y.1
Shen, Y.2
Gibbs, R.A.3
Nelson, D.L.4
-
5
-
-
0030580974
-
How many X-linked genes for non-specific mental retardation (MRX) are there?
-
Gedeon AK, Donnelly AJ, Mulley JC, Kerr B, Turner G. How many X-linked genes for non-specific mental retardation (MRX) are there? Am J Med Genet 1996;64:158-62.
-
(1996)
Am J Med Genet
, vol.64
, pp. 158-162
-
-
Gedeon, A.K.1
Donnelly, A.J.2
Mulley, J.C.3
Kerr, B.4
Turner, G.5
-
6
-
-
0030458716
-
Nonsyndromic X-linked mental retardation: Review and mapping of MRX29 to Xp21
-
Hane B, Schroer RJ, Arena JF, Lubs HA, Schwartz CE, Stevenson RE. Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21. Clin Genet 1996;50:176-83.
-
(1996)
Clin Genet
, vol.50
, pp. 176-183
-
-
Hane, B.1
Schroer, R.J.2
Arena, J.F.3
Lubs, H.A.4
Schwartz, C.E.5
Stevenson, R.E.6
-
7
-
-
0025085637
-
Allan-Herndon syndrome II. Linkage to DNA markers in Xq21
-
Schwartz CE, Ulmer J, Brown A, Pancoast I, Goodman HO, Stevenson RE. Allan-Herndon syndrome II. Linkage to DNA markers in Xq21. Am J Hum Genet 1990;47:454-9.
-
(1990)
Am J Hum Genet
, vol.47
, pp. 454-459
-
-
Schwartz, C.E.1
Ulmer, J.2
Brown, A.3
Pancoast, I.4
Goodman, H.O.5
Stevenson, R.E.6
-
8
-
-
0000981498
-
Report of the sixth international workshop on X chromosome mapping 1995
-
Nelson DL, Ballabio A, Cremers F, Monaco AP, Schlessinger D. Report of the sixth international workshop on X chromosome mapping 1995. Cytogenet Cell Genet 1995;71:308-26.
-
(1995)
Cytogenet Cell Genet
, vol.71
, pp. 308-326
-
-
Nelson, D.L.1
Ballabio, A.2
Cremers, F.3
Monaco, A.P.4
Schlessinger, D.5
-
9
-
-
0021344005
-
Easy calculations of lod scores and genetic risks on small computers
-
Lathrop GM, Lalouel JM. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 1984;36:460-5.
-
(1984)
Am J Hum Genet
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
10
-
-
0028937577
-
Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: Identification of a gene near FRAXE
-
Mulley JC. Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: identification of a gene near FRAXE. Am J Hum Genet 1995;56:907-14.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 907-914
-
-
Mulley, J.C.1
-
11
-
-
0021991210
-
An X-linked recessive basal ganglia disorder with mental retardation
-
Laxova R, Brown ES, Hogan K, Hecox K, Opitz JM. An X-linked recessive basal ganglia disorder with mental retardation. Am J Med Genet 1985;21:681-9.
-
(1985)
Am J Med Genet
, vol.21
, pp. 681-689
-
-
Laxova, R.1
Brown, E.S.2
Hogan, K.3
Hecox, K.4
Opitz, J.M.5
-
12
-
-
0026084867
-
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: Localization to Xq27.3-qter
-
Gregg RG, Metzenberg AB, Hogan K, Sekhon G, Laxova R. Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter. Genomics 1991;9:701-6.
-
(1991)
Genomics
, vol.9
, pp. 701-706
-
-
Gregg, R.G.1
Metzenberg, A.B.2
Hogan, K.3
Sekhon, G.4
Laxova, R.5
-
13
-
-
0029964708
-
PPM-X: A new X-linked mental retardation syndrome with psychosis, pyramidal signs and macroorchidism maps to Xq28
-
Lindsay S, Splitt M, Edney S, et al. PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs and macroorchidism maps to Xq28. Am J Hum Genet 1996;58:1120-6.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1120-1126
-
-
Lindsay, S.1
Splitt, M.2
Edney, S.3
-
14
-
-
0025884456
-
Localisation of the MRX3 gene for non-specific X linked mental retardation
-
Gedeon A, Kerr B, Mulley J, Turner G. Localisation of the MRX3 gene for non-specific X linked mental retardation. J Med Genet 1991;28:372-7.
-
(1991)
J Med Genet
, vol.28
, pp. 372-377
-
-
Gedeon, A.1
Kerr, B.2
Mulley, J.3
Turner, G.4
-
15
-
-
0343412332
-
X-linked mental retardation: Linkage results in five unrelated families
-
Moraine C, Dessay B, Toutain A, Briault S, Gendrot C, Ronce N. X-linked mental retardation: linkage results in five unrelated families. Am J Hum Genet 1994;55:A196.
-
(1994)
Am J Hum Genet
, vol.55
-
-
Moraine, C.1
Dessay, B.2
Toutain, A.3
Briault, S.4
Gendrot, C.5
Ronce, N.6
-
16
-
-
0026526250
-
Linkage to Xq28 in a family with non-specific X-linked recessive mental retardation
-
Nordstrom A, Penttinen M, von Koskull H. Linkage to Xq28 in a family with non-specific X-linked recessive mental retardation. Hum Genet 1992;90:263-6.
-
(1992)
Hum Genet
, vol.90
, pp. 263-266
-
-
Nordstrom, A.1
Penttinen, M.2
Von Koskull, H.3
-
17
-
-
0029950258
-
Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33)
-
Holinski-Feder E, Golla A, Rost I, Seidel H, Rittinger O, Meindl A. Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33). Am J Med Genet 1996;64:125-30.
-
(1996)
Am J Med Genet
, vol.64
, pp. 125-130
-
-
Holinski-Feder, E.1
Golla, A.2
Rost, I.3
Seidel, H.4
Rittinger, O.5
Meindl, A.6
-
18
-
-
0029949944
-
A gene for non-specific X-linked mental retardation is located in the distal segment of Xq28
-
Hamel BCJ, Kremer H, Wesby-van Swaay E, et al. A gene for non-specific X-linked mental retardation is located in the distal segment of Xq28. Am J Med Genet 1996;64:131-3.
-
(1996)
Am J Med Genet
, vol.64
, pp. 131-133
-
-
Hamel, B.C.J.1
Kremer, H.2
Wesby-van Swaay, E.3
-
19
-
-
0026683988
-
Nomenclature guidelines for X-linked recessive mental retardation
-
Mulley JC, Kerr B, Stevenson R, Lubs H. Nomenclature guidelines for X-linked recessive mental retardation. Am J Med Genet 1992;43:383-91.
-
(1992)
Am J Med Genet
, vol.43
, pp. 383-391
-
-
Mulley, J.C.1
Kerr, B.2
Stevenson, R.3
Lubs, H.4
-
20
-
-
0030580981
-
+2.71 lod score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X chromosome markers
-
Robledo R, Melis P, Siniscalco M, et al. +2.71 lod score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X chromosome markers. Am J Med Genet 1996;64:134-6.
-
(1996)
Am J Med Genet
, vol.64
, pp. 134-136
-
-
Robledo, R.1
Melis, P.2
Siniscalco, M.3
-
21
-
-
0029889132
-
The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule
-
Fransen E, Vits L, van Camp G, Willems PJ. The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule. Am J Med Genet 1996;64:73-7.
-
(1996)
Am J Med Genet
, vol.64
, pp. 73-77
-
-
Fransen, E.1
Vits, L.2
Van Camp, G.3
Willems, P.J.4
|