-
1
-
-
0005230111
-
Mental Retardation
-
Oski F, DeAngelis C, Feigin R, McMillan J, Warshaw J (eds): Philadelphia: J.B. Lippincott Co.
-
Accardo P, Capute A (1994): Mental Retardation. In Oski F, DeAngelis C, Feigin R, McMillan J, Warshaw J (eds): "Principles and Practice of Pediatrics," Philadelphia: J.B. Lippincott Co., pp 673-679.
-
(1994)
Principles and Practice of Pediatrics
, pp. 673-679
-
-
Accardo, P.1
Capute, A.2
-
2
-
-
33749733494
-
Ineontinentia pigmenti
-
Arrighi M (1955): Ineontinentia pigmenti. Bull Soc Franc Derm Syph 62: 206-208.
-
(1955)
Bull Soc Franc Derm Syph
, vol.62
, pp. 206-208
-
-
Arrighi, M.1
-
3
-
-
0016744065
-
Incontinentia pigmenti in a 21-year-old man
-
Bargman H, Wyse C (1975): Incontinentia pigmenti in a 21-year-old man. Arch Dermatol 111:1606-1608.
-
(1975)
Arch Dermatol
, vol.111
, pp. 1606-1608
-
-
Bargman, H.1
Wyse, C.2
-
5
-
-
0023276241
-
Gene for incontinentia pigmenti maps to band Xq11 with an (X,10)(p11,q22) translocation
-
Cannizzaro LA, Hecht F (1987): Gene for incontinentia pigmenti maps to band Xq11 with an (X,10)(p11,q22) translocation. Clin Genet 32:66-69.
-
(1987)
Clin Genet
, vol.32
, pp. 66-69
-
-
Cannizzaro, L.A.1
Hecht, F.2
-
6
-
-
0017260992
-
Incontinentia pigmenti: A world statistical analysis
-
Carney RG (1976): Incontinentia pigmenti: A world statistical analysis. Arch Dermatol 122:535-542.
-
(1976)
Arch Dermatol
, vol.122
, pp. 535-542
-
-
Carney, R.G.1
-
7
-
-
0038724518
-
Incontinentia pigmenti: Associated with changes in the posterior chamber of the eye
-
Cole J, Cole H (1959): Incontinentia pigmenti: Associated with changes in the posterior chamber of the eye. Am J Ophthalmol 47:321-328.
-
(1959)
Am J Ophthalmol
, vol.47
, pp. 321-328
-
-
Cole, J.1
Cole, H.2
-
8
-
-
33749797711
-
Incontinentia pigmenti
-
Cormie R (1952): Incontinentia pigmenti. Brit J Dermatol 65:285.
-
(1952)
Brit J Dermatol
, vol.65
, pp. 285
-
-
Cormie, R.1
-
9
-
-
33749765906
-
Incontinentia pigmenti: Report of six cases
-
Cramer J, Schmidt W (1955): Incontinentia pigmenti: Report of six cases. Arch Derm 71:699-702.
-
(1955)
Arch Derm
, vol.71
, pp. 699-702
-
-
Cramer, J.1
Schmidt, W.2
-
10
-
-
0030752675
-
Mosaic Trisomy 22: A case presentation and literature review of trisomy 22 phenotypes
-
Crowe C, Schwartz S, Black C, Jaswaney V (1997): Mosaic Trisomy 22: A case presentation and literature review of trisomy 22 phenotypes. Am J Med Genet 71:406-413.
-
(1997)
Am J Med Genet
, vol.71
, pp. 406-413
-
-
Crowe, C.1
Schwartz, S.2
Black, C.3
Jaswaney, V.4
-
11
-
-
0013802626
-
The genetics of incontinentia pigmenti
-
Curth H, Warburton D (1965): The genetics of incontinentia pigmenti. Arch Dermatol 92:229-235.
-
(1965)
Arch Dermatol
, vol.92
, pp. 229-235
-
-
Curth, H.1
Warburton, D.2
-
13
-
-
0027204207
-
Incontinentia pigmenti: Transmission from father to daughter
-
Emery M, Siegfried E, Stone M, Stone E, Patil S (1993): Incontinentia pigmenti: Transmission from father to daughter. J Am Acad Dermatol 29:368-372.
-
(1993)
J Am Acad Dermatol
, vol.29
, pp. 368-372
-
-
Emery, M.1
Siegfried, E.2
Stone, M.3
Stone, E.4
Patil, S.5
-
16
-
-
0002665724
-
A propos de l"Incontinentia pigmenti", délimitation de deux syndrome différents figurant sous le même terme
-
Franceschetti A, Jadassohn W (1954): A propos de l"Incontinentia pigmenti", délimitation de deux syndrome différents figurant sous le même terme. Dermatologica 108:1-28.
-
(1954)
Dermatologica
, vol.108
, pp. 1-28
-
-
Franceschetti, A.1
Jadassohn, W.2
-
18
-
-
0025368786
-
Incontinentia pigmenti: XXY male with family history
-
Garcia-Dorado J, De Unamo P, Fernandez-Lopez E, Salazar Velos J, Armijo M (1990): Incontinentia pigmenti: XXY male with family history. Clin Genet 38:128-38.
-
(1990)
Clin Genet
, vol.38
, pp. 128-138
-
-
Garcia-Dorado, J.1
De Unamo, P.2
Fernandez-Lopez, E.3
Salazar Velos, J.4
Armijo, M.5
-
19
-
-
33749719002
-
Cystic hygroma as a probable feature in male fetuses with incontinentia pigmenti
-
Garza J, Miller ME (1992): Cystic hygroma as a probable feature in male fetuses with incontinentia pigmenti (Abstract). Am J Hum Genet 51 (Supplement):A256.
-
(1992)
Am J Hum Genet
, vol.51
, Issue.SUPPL.
-
-
Garza, J.1
Miller, M.E.2
-
21
-
-
0020030585
-
Incontinentia pigmenti in Arizona Indians including transmission from mother to son inconsistent with the half chromatid mutation model
-
Hecht F, Hecht B, Austin W (1982): Incontinentia pigmenti in Arizona Indians including transmission from mother to son inconsistent with the half chromatid mutation model. Clin Genet 21:293-296.
-
(1982)
Clin Genet
, vol.21
, pp. 293-296
-
-
Hecht, F.1
Hecht, B.2
Austin, W.3
-
22
-
-
0014533409
-
Incontinentia pigmenti (Sulzberger-Bloch type) report in a male
-
Khanna K, Veliath A, Bedi T (1969): Incontinentia pigmenti (Sulzberger-Bloch type) report in a male. Indian J Pediatr 36:224-225.
-
(1969)
Indian J Pediatr
, vol.36
, pp. 224-225
-
-
Khanna, K.1
Veliath, A.2
Bedi, T.3
-
23
-
-
33749760721
-
Über zwei japanische Fälle einer eigenartigen retikulären Pigmentierung
-
Kitamura V, Hirako T (1955): Über zwei japanische Fälle einer eigenartigen retikulären Pigmentierung. Dermatologica 110:97-107.
-
(1955)
Dermatologica
, vol.110
, pp. 97-107
-
-
Kitamura, V.1
Hirako, T.2
-
24
-
-
0017360316
-
Klinefelter's syndrome and incontinentia pigmenti Bloch-Sulzberger
-
Kunze J, Frenzel U, Hüttig E, Grosse F-R, Wiedemann H-R (1977): Klinefelter's syndrome and incontinentia pigmenti Bloch-Sulzberger. Hum Genet 35:237-240.
-
(1977)
Hum Genet
, vol.35
, pp. 237-240
-
-
Kunze, J.1
Frenzel, U.2
Hüttig, E.3
Grosse, F.-R.4
Wiedemann, H.-R.5
-
25
-
-
0020451969
-
Studies of a family with incontinentia pigmenti variably expressed in both sexes
-
Kurczynski T, Berns J, Johnson W (1982): Studies of a family with incontinentia pigmenti variably expressed in both sexes. J Med Genet 19: 447-451.
-
(1982)
J Med Genet
, vol.19
, pp. 447-451
-
-
Kurczynski, T.1
Berns, J.2
Johnson, W.3
-
26
-
-
33749701674
-
Incontinentia pigmenti
-
Lahiri K (1955): Incontinentia pigmenti. Br J Dermatol 67:310-312.
-
(1955)
Br J Dermatol
, vol.67
, pp. 310-312
-
-
Lahiri, K.1
-
27
-
-
0027403249
-
Incontinentia pigmenti (Bloch-Sulzberger syndrome)
-
Landy SJ, Donnai D (1993): Incontinentia pigmenti (Bloch-Sulzberger syndrome). J Med Genet 53-59.
-
(1993)
J Med Genet
, pp. 53-59
-
-
Landy, S.J.1
Donnai, D.2
-
28
-
-
0002563987
-
Zur Genetik der Incontinentia pigmenti
-
Lenz W (1961): Zur Genetik der Incontinentia pigmenti. Ann Paediatr 196:149-165.
-
(1961)
Ann Paediatr
, vol.196
, pp. 149-165
-
-
Lenz, W.1
-
29
-
-
0016548130
-
Half chromatid mutations may explain incontinentia pigmenti in males
-
Lenz W (1975): Half chromatid mutations may explain incontinentia pigmenti in males. Am J Hum Genet 27:690-691.
-
(1975)
Am J Hum Genet
, vol.27
, pp. 690-691
-
-
Lenz, W.1
-
31
-
-
33749703069
-
Incontinentia pigmenti
-
Luscombe H (1959): Incontinentia pigmenti. Ann Dermatol Syphiligr 80: 125-126.
-
(1959)
Ann Dermatol Syphiligr
, vol.80
, pp. 125-126
-
-
Luscombe, H.1
-
32
-
-
33749714926
-
Incontinentia pigmenti bei einem 2 3/4 jährigen Knaben
-
Moncorps C (1936): Incontinentia pigmenti bei einem 2 3/4 jährigen Knaben. Zbl Haut-GeschlKr 54:291.
-
(1936)
Zbl Haut-GeschlKr
, vol.54
, pp. 291
-
-
Moncorps, C.1
-
33
-
-
0002625956
-
Familiärer Chromatophorennävus
-
Naegeli O (1927): Familiärer Chromatophorennävus. Schweiz Med Wocbenschr 57:48.
-
(1927)
Schweiz Med Wocbenschr
, vol.57
, pp. 48
-
-
Naegeli, O.1
-
35
-
-
0021892811
-
Incontinentia pigmenti: A longitudinal study
-
O'Brien J, Feingold M (1985): Incontinentia pigmenti: A longitudinal study. Am J Dis Child 139:711-712.
-
(1985)
Am J Dis Child
, vol.139
, pp. 711-712
-
-
O'Brien, J.1
Feingold, M.2
-
36
-
-
0346107803
-
Incontinentia pigmenti
-
Oldfelt V (1959): Incontinentia pigmenti. J Pediatrics 54:446-458.
-
(1959)
J Pediatrics
, vol.54
, pp. 446-458
-
-
Oldfelt, V.1
-
38
-
-
0014455358
-
Incontinentia pigmenti in a newborn boy
-
Stockh
-
Pallisgaard D (1969): Incontinentia pigmenti in a newborn boy. Acta Dermatol Venereol (Stockh) 49:197-201.
-
(1969)
Acta Dermatol Venereol
, vol.49
, pp. 197-201
-
-
Pallisgaard, D.1
-
39
-
-
0023861047
-
Chromosomal instability in incontinentia pigmenti: Study of four families
-
Pallott R, Dalpra L (1988): Chromosomal instability in incontinentia pigmenti: study of four families. Ann Genet 31:27-31.
-
(1988)
Ann Genet
, vol.31
, pp. 27-31
-
-
Pallott, R.1
Dalpra, L.2
-
40
-
-
33749752401
-
Das Syndrom der Incontinentia pigmenti Bloch-Siemens
-
Pfeiffer RA (1959): Das Syndrom der Incontinentia pigmenti Bloch-Siemens. Munch Med Wochenschr 101:2312-2316.
-
(1959)
Munch Med Wochenschr
, vol.101
, pp. 2312-2316
-
-
Pfeiffer, R.A.1
-
41
-
-
0002676227
-
Zur Frage der Vererbung der Incontinentia pigmenti Bloch-Siemens
-
Pfeiffer RA (1960): Zur Frage der Vererbung der Incontinentia pigmenti Bloch-Siemens. Zeit Menschlich Ver Konstitutiouslehre 35:469-493.
-
(1960)
Zeit Menschlich Ver Konstitutiouslehre
, vol.35
, pp. 469-493
-
-
Pfeiffer, R.A.1
-
43
-
-
33749751743
-
Incontinentia pigmenti in three siblings: Discussion
-
Pinkus H (1957): Incontinentia pigmenti in three siblings: Discussion. Arch Dermatol 75:144-145.
-
(1957)
Arch Dermatol
, vol.75
, pp. 144-145
-
-
Pinkus, H.1
-
44
-
-
0022294194
-
Incontinentia pigmenti, analysis of 15 cases
-
Pongprasit P, Chittinand S, Lerchawanakul A, Chermsiriwat S (1985): Incontinentia pigmenti, analysis of 15 cases. J Med Assoc Thai 68:630-637.
-
(1985)
J Med Assoc Thai
, vol.68
, pp. 630-637
-
-
Pongprasit, P.1
Chittinand, S.2
Lerchawanakul, A.3
Chermsiriwat, S.4
-
46
-
-
0031973510
-
Incontinentia pigmenti in a newborn male infant with DNA confirmation
-
Roberts JL, Morrow B, Vega-Rich C, Salafia CM, Nitowsky HM (1998): Incontinentia pigmenti in a newborn male infant with DNA confirmation. Am J Med Genet 75:159-163.
-
(1998)
Am J Med Genet
, vol.75
, pp. 159-163
-
-
Roberts, J.L.1
Morrow, B.2
Vega-Rich, C.3
Salafia, C.M.4
Nitowsky, H.M.5
-
47
-
-
33749755484
-
A propose de deux cas d'lncontinentia pigmenti
-
Rollier M (1959): A propose de deux cas d'lncontinentia pigmenti. Soc Derm Syphil 28:122-125.
-
(1959)
Soc Derm Syphil
, vol.28
, pp. 122-125
-
-
Rollier, M.1
-
48
-
-
33749745732
-
Incontinentia pigmenti
-
Scheurmann H (1939): Incontinentia pigmenti. Zbl Hautkrkh 62:615.
-
(1939)
Zbl Hautkrkh
, vol.62
, pp. 615
-
-
Scheurmann, H.1
-
49
-
-
0024651107
-
The gene for incontinentia pigmenti is assigned to Xq28
-
Sefiani A, Abel L, Heuertz S, Sinnett D, Lavergne L, Labuda D, Hors-Cayla MC (1989): The gene for incontinentia pigmenti is assigned to Xq28. Genomics 4:427-429.
-
(1989)
Genomics
, vol.4
, pp. 427-429
-
-
Sefiani, A.1
Abel, L.2
Heuertz, S.3
Sinnett, D.4
Lavergne, L.5
Labuda, D.6
Hors-Cayla, M.C.7
-
50
-
-
33749728108
-
Über ein neues Syndrom multipler Abartung: Pigmentanomalie, kongenitale ektodermal Dysplasie, Nebennierenmarkaplasie
-
Seidlemayer H (1943): Über ein neues Syndrom multipler Abartung: Pigmentanomalie, kongenitale ektodermal Dysplasie, Nebennierenmarkaplasie. Z Kinderheilk 63:451-487.
-
(1943)
Z Kinderheilk
, vol.63
, pp. 451-487
-
-
Seidlemayer, H.1
-
51
-
-
0021333510
-
Incontinentia pigmenti in a father and his daughter
-
Sommer A, Liu P (1983): Incontinentia pigmenti in a father and his daughter. Am J Med Genet 17:655-659.
-
(1983)
Am J Med Genet
, vol.17
, pp. 655-659
-
-
Sommer, A.1
Liu, P.2
-
52
-
-
0012433415
-
Incontinentia pigmenti (Bloch-Sulzberger): Report of an additional case, with comment on possible relation to a new syndrome of familial and congenital anomalies
-
Sulzberger M (1938): Incontinentia pigmenti (Bloch-Sulzberger): Report of an additional case, with comment on possible relation to a new syndrome of familial and congenital anomalies. Arch Derm Syph 38:57-69.
-
(1938)
Arch Derm Syph
, vol.38
, pp. 57-69
-
-
Sulzberger, M.1
-
53
-
-
0002399594
-
Über eine bisher nicht beschriebene congenitale pigmentanomalie (Incontinentia Pigmenti)
-
Berl
-
Sulzberger MB (1928): Über eine bisher nicht beschriebene congenitale pigmentanomalie (Incontinentia Pigmenti). Arch Dermatol Syph (Berl) 154:19-32.
-
(1928)
Arch Dermatol Syph
, vol.154
, pp. 19-32
-
-
Sulzberger, M.B.1
-
54
-
-
0025278925
-
Pigmentary abnormalities and mosaicism for chromosomal aberration: Association with clinical features similar to hypomelanosis of Ito
-
Sybert VP, Pagon RA, Donlan M, Bradley CM (1990): Pigmentary abnormalities and mosaicism for chromosomal aberration: Association with clinical features similar to hypomelanosis of Ito. J Pediatr 116:581-586.
-
(1990)
J Pediatr
, vol.116
, pp. 581-586
-
-
Sybert, V.P.1
Pagon, R.A.2
Donlan, M.3
Bradley, C.M.4
-
55
-
-
0027976079
-
Unstable pre-mutation may explain mosaic disease expression of incontinentia pigmenti in males
-
Traupe H, Vehring K-H (1994): Unstable pre-mutation may explain mosaic disease expression of incontinentia pigmenti in males. Am J Med Genet 49:397-398.
-
(1994)
Am J Med Genet
, vol.49
, pp. 397-398
-
-
Traupe, H.1
Vehring, K.-H.2
-
57
-
-
0027500850
-
Incontinentia pigmenti in an infant boy
-
Vehring K-H, Kurlemann G, Traupe H, Bonsmann G, Gerding H, Möllmann S, Hamm H (1993): Incontinentia pigmenti in an infant boy. Hautarzt 44:726-730.
-
(1993)
Hautarzt
, vol.44
, pp. 726-730
-
-
Vehring, K.-H.1
Kurlemann, G.2
Traupe, H.3
Bonsmann, G.4
Gerding, H.5
Möllmann, S.6
Hamm, H.7
-
58
-
-
0020518307
-
X-linked dominant inherited diseases with lethality in hemizygous males
-
Wettke-Schäfer R, Kanter G (1983): X-linked dominant inherited diseases with lethality in hemizygous males. Hum Genet 64:1-23.
-
(1983)
Hum Genet
, vol.64
, pp. 1-23
-
-
Wettke-Schäfer, R.1
Kanter, G.2
|