-
1
-
-
0003897579
-
-
Baltimore: Williams and Wilkins
-
Spitz J L. Genodermatoses. Baltimore: Williams and Wilkins, 1996:64.
-
(1996)
Genodermatoses
, pp. 64
-
-
Spitz, J.L.1
-
2
-
-
0032543269
-
Male cases of incontinentia pigmenti: Case report and review
-
Scheuerle A E. Male cases of incontinentia pigmenti: case report and review. Am J Med Genet 1998; 77:201-18.
-
(1998)
Am J Med Genet
, vol.77
, pp. 201-218
-
-
Scheuerle, A.E.1
-
3
-
-
0034713270
-
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium
-
Smahi A, Courtois G. Vabres P, Yamaoka S, Heuertz S, Munnich A, et al. Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium. Nature 2000; 405:466-72.
-
(2000)
Nature
, vol.405
, pp. 466-472
-
-
Smahi, A.1
Courtois, G.2
Vabres, P.3
Yamaoka, S.4
Heuertz, S.5
Munnich, A.6
-
4
-
-
0017260992
-
Incontinentia pigmenti: A world statistical analysis
-
Carney R G. Incontinentia pigmenti: A world statistical analysis. Arch Dermatol 1976; 112:535-42.
-
(1976)
Arch Dermatol
, vol.112
, pp. 535-542
-
-
Carney, R.G.1
-
5
-
-
0032788145
-
Functional X-chromosomal mosaicism of the skin: Rudolf Happle and the lines of Alfred Blaschko
-
Traupe H. Functional X-chromosomal mosaicism of the skin: Rudolf Happle and the lines of Alfred Blaschko. Am J Med Genet 1999; 85:324-9.
-
(1999)
Am J Med Genet
, vol.85
, pp. 324-329
-
-
Traupe, H.1
-
6
-
-
7144223296
-
Gene action in the X-chromosome of the mouse (Mus musculus L.)
-
Lyon M. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature 1961; 190:372-3.
-
(1961)
Nature
, vol.190
, pp. 372-373
-
-
Lyon, M.1
-
7
-
-
0022416999
-
Lyonization and the lines of Blaschko
-
Happle R. Lyonization and the lines of Blaschko. Hum Genet 1985; 70:200-6.
-
(1985)
Hum Genet
, vol.70
, pp. 200-206
-
-
Happle, R.1
-
8
-
-
0020518307
-
X-linked dominant inherited diseases with lethality in hemizygous males
-
Wettke-Schäfer R, Kantner G. X-linked dominant inherited diseases with lethality in hemizygous males. Hum Genet 1983; 64:1-23.
-
(1983)
Hum Genet
, vol.64
, pp. 1-23
-
-
Wettke-Schäfer, R.1
Kantner, G.2
-
9
-
-
0016670103
-
Incontinentia pigmenti
-
Iancu T, Komlos L, Shabtay F, Elian E, Halbrecht L, Book J A. Incontinentia pigmenti. Clin Genet 1975; 7:103-10.
-
(1975)
Clin Genet
, vol.7
, pp. 103-110
-
-
Iancu, T.1
Komlos, L.2
Shabtay, F.3
Elian, E.4
Halbrecht, L.5
Book, J.A.6
-
10
-
-
0018900717
-
Incontinentia pigmenti: A four-generation study
-
Wiklund D A, Weston W L. Incontinentia pigmenti: a four-generation study. Arch Dermatol 1980; 116:701-3.
-
(1980)
Arch Dermatol
, vol.116
, pp. 701-703
-
-
Wiklund, D.A.1
Weston, W.L.2
-
11
-
-
0021892811
-
Incontinentia pigmenti: A longitudinal study
-
O'Brien J E, Feingold M. Incontinentia pigmenti: a longitudinal study. Am J Dis Child 1985; 139:711-2.
-
(1985)
Am J Dis Child
, vol.139
, pp. 711-712
-
-
O'Brien, J.E.1
Feingold, M.2
-
12
-
-
0027452134
-
Mosaicism in human skin: Understanding the patterns and mechanisms
-
Happle R. Mosaicism in human skin: Understanding the patterns and mechanisms. Arch Dermatol 1993; 129:1460-70.
-
(1993)
Arch Dermatol
, vol.129
, pp. 1460-1470
-
-
Happle, R.1
-
13
-
-
0021258993
-
Wie verlaufen die Blaschko-Linien am behaarten kopf?
-
Happle R, Fuhrmann-Rieger A, Fuhrmann W. Wie verlaufen die Blaschko-Linien am behaarten Kopf? Hautarzt 1984; 35:366-9.
-
(1984)
Hautarzt
, vol.35
, pp. 366-369
-
-
Happle, R.1
Fuhrmann-Rieger, A.2
Fuhrmann, W.3
-
16
-
-
0016548130
-
Half chromatid mutations may explain incontinentia pigmenti in males
-
Lenz W. Half chromatid mutations may explain incontinentia pigmenti in males. Am J Hum Genet 1975; 27:690-1.
-
(1975)
Am J Hum Genet
, vol.27
, pp. 690-691
-
-
Lenz, W.1
-
17
-
-
0018080569
-
Incontinentia pigmenti: Report of a case with persistent activity into adult life
-
Barnes C M. Incontinentia pigmenti: report of a case with persistent activity into adult life. Cutis 1978; 22:621-4.
-
(1978)
Cutis
, vol.22
, pp. 621-624
-
-
Barnes, C.M.1
-
18
-
-
0022341303
-
X inactivation patterns in two syndromes with probable X-linked dominant, male lethal inheritance
-
Wieacker P, Zimmer J, Ropers H H. X inactivation patterns in two syndromes with probable X-linked dominant, male lethal inheritance. Clin Genet 1985; 28:238-42.
-
(1985)
Clin Genet
, vol.28
, pp. 238-242
-
-
Wieacker, P.1
Zimmer, J.2
Ropers, H.H.3
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