-
1
-
-
84995840997
-
A syndrome of infantilism, congenital webbed neck and cubitus valgus
-
Turner HH. A syndrome of infantilism, congenital webbed neck and cubitus valgus. Endocrinology 1938;23:566.
-
(1938)
Endocrinology
, vol.23
, pp. 566
-
-
Turner, H.H.1
-
2
-
-
0026574505
-
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding
-
Jacobs PA, Browne C, Gregson N, Joyce C, White H. Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding. J Med Genet 1992;29:103-8.
-
(1992)
J Med Genet
, vol.29
, pp. 103-108
-
-
Jacobs, P.A.1
Browne, C.2
Gregson, N.3
Joyce, C.4
White, H.5
-
3
-
-
0014532704
-
Les manifestations ophtalmologiques du syndrome de Turner
-
Cordier TJ, Reny A. Les manifestations ophtalmologiques du syndrome de Turner. Arch Ophtalmol (Paris) 1969;29: 565-74.
-
(1969)
Arch Ophtalmol (Paris)
, vol.29
, pp. 565-574
-
-
Cordier, T.J.1
Reny, A.2
-
4
-
-
0013941311
-
Eye signs in Turner's syndrome
-
Lessel S, Forbes AP. Eye signs in Turner's syndrome. Arch Ophthalmol 1966;76:211-3.
-
(1966)
Arch Ophthalmol
, vol.76
, pp. 211-213
-
-
Lessel, S.1
Forbes, A.P.2
-
5
-
-
0014992863
-
Turner's syndrome
-
Wesson ME. Turner's syndrome. Am Orthopt J 1971;21:50-6.
-
(1971)
Am Orthopt J
, vol.21
, pp. 50-56
-
-
Wesson, M.E.1
-
7
-
-
0021167450
-
Ocular findings in Turner syndrome
-
Chrousos GA, Ross JL, Chrousos G, Chu FC, Kenigsberg D, Cutler G, Jr, et al. Ocular findings in Turner syndrome. Ophthalmology 1984;91:926-8.
-
(1984)
Ophthalmology
, vol.91
, pp. 926-928
-
-
Chrousos, G.A.1
Ross, J.L.2
Chrousos, G.3
Chu, F.C.4
Kenigsberg, D.5
Cutler Jr., G.6
-
8
-
-
0025153268
-
Eyes and the Turner syndrome: A nationwide survey
-
Masters MC. Eyes and the Turner syndrome: a nationwide survey. Br Orthopt J 1990;46:7-17.
-
(1990)
Br Orthopt J
, vol.46
, pp. 7-17
-
-
Masters, M.C.1
-
10
-
-
0001156859
-
Sex chromosome abnormalities
-
Rimoin D, Connor JM, Pyeritz RE, eds. Edinburgh: Churchill Livingstone
-
Robinson A, de la Chapelle A. Sex chromosome abnormalities. In: Rimoin D, Connor JM, Pyeritz RE, eds. Principles and practice of medical genetics. Edinburgh: Churchill Livingstone, 1996:973-97.
-
(1996)
Principles and Practice of Medical Genetics
, pp. 973-997
-
-
Robinson, A.1
De La Chapelle, A.2
-
11
-
-
8544259733
-
Classical chromosome disorders
-
Yunis JJ, ed. New York: Academic Press
-
Gorlin RJ. Classical chromosome disorders. In: Yunis JJ, ed. New chromosome syndromes. New York: Academic Press, 1977:59-117.
-
(1977)
New Chromosome Syndromes
, pp. 59-117
-
-
Gorlin, R.J.1
-
13
-
-
0025740563
-
The ocular changes of incondnentia pigmenti achromians (hypomelanosis of Ito)
-
Weaver RG, Martin T, Zanolli MD. The ocular changes of incondnentia pigmenti achromians (hypomelanosis of Ito). J Pediatr Ophthalmol Strabismus 1991;28:160-3.
-
(1991)
J Pediatr Ophthalmol Strabismus
, vol.28
, pp. 160-163
-
-
Weaver, R.G.1
Martin, T.2
Zanolli, M.D.3
-
15
-
-
0027418712
-
Epigenetic inheritance in mammals
-
Lyon MF. Epigenetic inheritance in mammals. Trends Genet 1993;9:123-8.
-
(1993)
Trends Genet
, vol.9
, pp. 123-128
-
-
Lyon, M.F.1
-
16
-
-
0023816813
-
Hypomelanosis of Ito: A manifestation of mosaicism or chimerism
-
Donnai D, Read AP, McKeown C, Andrews T. Hypomelanosis of Ito: a manifestation of mosaicism or chimerism. J Med Genet 1988;25:809-18.
-
(1988)
J Med Genet
, vol.25
, pp. 809-818
-
-
Donnai, D.1
Read, A.P.2
McKeown, C.3
Andrews, T.4
-
17
-
-
0024419361
-
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism
-
Thomas IT, Frias JL, Cantu ES, Lafer CZ, Flannery DB, Graham JG. Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism. Am J Hum Genet 1989;45:193-205.
-
(1989)
Am J Hum Genet
, vol.45
, pp. 193-205
-
-
Thomas, I.T.1
Frias, J.L.2
Cantu, E.S.3
Lafer, C.Z.4
Flannery, D.B.5
Graham, J.G.6
-
18
-
-
0027403249
-
Incontinentia pigmenati (Bloch-Sulzberger syndrome)
-
Landy SJ, Donnai D. Incontinentia pigmenati (Bloch-Sulzberger syndrome). J Med Genet 1993;30:53-9.
-
(1993)
J Med Genet
, vol.30
, pp. 53-59
-
-
Landy, S.J.1
Donnai, D.2
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