-
1
-
-
0021592933
-
Linkage analysis of X‐linked mental retardation with and without fragile‐X using Factor IX gene probe
-
Choo KH, George D, Filby G, Halliday JL, Leversha M, Webb G, Danks DM [ 1984 ]: Linkage analysis of X‐linked mental retardation with and without fragile‐X using Factor IX gene probe. Lancet ii: 349.
-
(1984)
Lancet
, vol.ii
, pp. 349
-
-
Choo, KH1
George, D2
Filby, G3
Halliday, JL4
Leversha, M5
Webb, G6
Danks, DM7
-
2
-
-
85068950077
-
Report of the committee on methods of linkage analysis and reporting. 8th International Workshop on Human Gene Mapping
-
Conneally PM, Edwards JH, Kidd KK, Lalouel JM, Morton NE, Ott J, White R (1985): Report of the committee on methods of linkage analysis and reporting. 8th International Workshop on Human Gene Mapping. Cytogenet Cell Genet 40: 356–359.
-
(1985)
Cytogenet Cell Genet
, vol.40
, pp. 356-359
-
-
Conneally, PM1
Edwards, JH2
Kidd, KK3
Lalouel, JM4
Morton, NE5
Ott, J6
White, R7
-
3
-
-
0019193212
-
Non‐specific X‐linked mental retardation II: The frequency in British Columbia
-
Herbst DS, Miller JR (1980): Non‐specific X‐linked mental retardation II: The frequency in British Columbia. Am J Med Genet 7: 461–469.
-
(1980)
Am J Med Genet
, vol.7
, pp. 461-469
-
-
Herbst, DS1
Miller, JR2
-
4
-
-
0017359223
-
Colchester revisted: A genetic study of mental defect
-
Morton NE, Rao DC, Lang‐Brown H, MacLean CJ, Bart RC, Lew R (1977): Colchester revisted: A genetic study of mental defect. J Med Genet 14: 1–9.
-
(1977)
J Med Genet
, vol.14
, pp. 1-9
-
-
Morton, NE1
Rao, DC2
Lang‐Brown, H3
MacLean, CJ4
Bart, RC5
Lew, R6
-
5
-
-
0023212670
-
Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14
-
Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR (1987): Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14. Am J Med Genet 27: 435–448.
-
(1987)
Am J Med Genet
, vol.27
, pp. 435-448
-
-
Mulley, JC1
Gedeon, AK2
Thorn, KA3
Bates, LJ4
Sutherland, GR5
-
6
-
-
0016302483
-
Estimation of the recombination fraction in human pedigrees: Efficient computation of the likelihood for human linkage studies
-
Ott J (1974): Estimation of the recombination fraction in human pedigrees: Efficient computation of the likelihood for human linkage studies. Am J Hum Genet 26: 588–597.
-
(1974)
Am J Hum Genet
, vol.26
, pp. 588-597
-
-
Ott, J1
-
7
-
-
0003555486
-
Fragile Sites on Human Chromosomes
-
Sutherland GR, Hecht F (1985): “ Fragile Sites on Human Chromosomes.” New York: Oxford University Press.
-
(1985)
-
-
Sutherland, GR1
Hecht, F2
-
8
-
-
0015012442
-
X‐linked mental retardation without physical abnormality: Renpenning's syndrome
-
Turner G, Turner B, Collins E (1971): X‐linked mental retardation without physical abnormality: Renpenning's syndrome. Dev Med Child Neurol 13: 71–78.
-
(1971)
Dev Med Child Neurol
, vol.13
, pp. 71-78
-
-
Turner, G1
Turner, B2
Collins, E3
-
9
-
-
0022201820
-
Report of the committee on human gene mapping by recombinant DNA techniques. 8th International Workshop on Human Gene Mapping
-
Willard HF, Skolnick MH, Pearson PL, Mandel JL (1985): Report of the committee on human gene mapping by recombinant DNA techniques. 8th International Workshop on Human Gene Mapping. Cytogenet Cell Genet 40: 360–489.
-
(1985)
Cytogenet Cell Genet
, vol.40
, pp. 360-489
-
-
Willard, HF1
Skolnick, MH2
Pearson, PL3
Mandel, JL4
|