-
3
-
-
0022416999
-
Lyonization and the lines of Blaschko
-
Happle R. Lyonization and the lines of Blaschko. Hum Genet. 1985;70:200-206.
-
(1985)
Hum Genet
, vol.70
, pp. 200-206
-
-
Happle, R.1
-
4
-
-
0023319298
-
Lethal genes surviving by mosaicism: A possible explanation for sporadic birth defects involving the skin
-
Happle R. Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin. Am Acad Dermatol. 1987;16:899-906.
-
(1987)
Am Acad Dermatol
, vol.16
, pp. 899-906
-
-
Happle, R.1
-
5
-
-
0027200119
-
Pigmentary patterns associated with human mosaicism: A proposed classification
-
Happle R. Pigmentary patterns associated with human mosaicism: a proposed classification. Eur J Dermatol. 1993;3:170-174.
-
(1993)
Eur J Dermatol
, vol.3
, pp. 170-174
-
-
Happle, R.1
-
6
-
-
0027452134
-
Mosaicism in human skin
-
Happle R. Mosaicism in human skin. Arch Dermatol. 1993;129:1460-1470.
-
(1993)
Arch Dermatol
, vol.129
, pp. 1460-1470
-
-
Happle, R.1
-
7
-
-
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
-
8
-
-
0343227733
-
Cutaneous findings in mosaicism and chimerism
-
Loomis CA, Orlow SJ. Cutaneous findings in mosaicism and chimerism. Curr Opin Dermatol. 1996;3:87-92.
-
(1996)
Curr Opin Dermatol
, vol.3
, pp. 87-92
-
-
Loomis, C.A.1
Orlow, S.J.2
-
9
-
-
0015605643
-
Hypomelanosis of Ito (incontinentia pigmentia achromians): Report of three cases and review of the literature
-
Jelinek JE, Bart RS, Schiff GM. Hypomelanosis of Ito (incontinentia pigmentia achromians): report of three cases and review of the literature. Arch Dermatol. 1973;107:596-601.
-
(1973)
Arch Dermatol
, vol.107
, pp. 596-601
-
-
Jelinek, J.E.1
Bart, R.S.2
Schiff, G.M.3
-
10
-
-
0003076242
-
Incontinentia pigmenti achromians: A singular case of nevus depigmentosus systematicus bilateralis
-
Ito M. Incontinentia pigmenti achromians: a singular case of nevus depigmentosus systematicus bilateralis. Tohoku J Exp Med. 1952;55:57-59.
-
(1952)
Tohoku J Exp Med
, vol.55
, pp. 57-59
-
-
Ito, M.1
-
11
-
-
0025609098
-
Hypomelanosis of Ito and hemimegalencephaly
-
Battistella PA, Peserico A, Bertoli P, Drigo P, Laverda AM, Casara GL. Hypomelanosis of Ito and hemimegalencephaly. Childs Nerv Syst. 1990;6:421-423.
-
(1990)
Childs Nerv Syst
, vol.6
, pp. 421-423
-
-
Battistella, P.A.1
Peserico, A.2
Bertoli, P.3
Drigo, P.4
Laverda, A.M.5
Casara, G.L.6
-
12
-
-
0027160489
-
Central nervous system lesions in hypomelanosis of Ito: An MRI and pathologic study
-
Malherbe V, Pariente D, Tardieu M, et al. Central nervous system lesions in hypomelanosis of Ito: an MRI and pathologic study. J Neurol. 1993;240:302-304.
-
(1993)
J Neurol
, vol.240
, pp. 302-304
-
-
Malherbe, V.1
Pariente, D.2
Tardieu, M.3
-
13
-
-
0027282360
-
Autism and hypomelanosis of Ito in twins
-
Zappella M. Autism and hypomelanosis of Ito in twins. Dev Med Child Neurol. 1993;35:826-832
-
(1993)
Dev Med Child Neurol
, vol.35
, pp. 826-832
-
-
Zappella, M.1
-
15
-
-
0021668842
-
Congenital craniofacial dysmorphosis associated with Ito's syndrome (incontinentia pigmenti achromians): A case report
-
Stricker M, Meley JM, Chassagne F, Beurey J. Congenital craniofacial dysmorphosis associated with Ito's syndrome (incontinentia pigmenti achromians): a case report. Br J Plast Surg. 1984;37:472-476.
-
(1984)
Br J Plast Surg
, vol.37
, pp. 472-476
-
-
Stricker, M.1
Meley, J.M.2
Chassagne, F.3
Beurey, J.4
-
17
-
-
0019352463
-
Hypomelanosis of Ito: Report of a case and review of the literature
-
Buzas JW, Sina B, Burnett JW. Hypomelanosis of Ito: report of a case and review of the literature. Am Acad Dermatol. 1981;4:195-204.
-
(1981)
Am Acad Dermatol
, vol.4
, pp. 195-204
-
-
Buzas, J.W.1
Sina, B.2
Burnett, J.W.3
-
19
-
-
0029008279
-
Neurocutaneous syndromes associated with pigmentary skin lesions
-
Zvulunov A, Esterly NB. Neurocutaneous syndromes associated with pigmentary skin lesions. J Am Acad Dermatol. 1995;32:915-935.
-
(1995)
J Am Acad Dermatol
, vol.32
, pp. 915-935
-
-
Zvulunov, A.1
Esterly, N.B.2
-
20
-
-
0017336045
-
Hypomelanosis of Ito (incontinentia pigmenti achromians): A neurocutaneous syndrome
-
Schwartz MF, Esterly NB, Fretzin DF, Pergament E, Rozenfeld IH. Hypomelanosis of Ito (incontinentia pigmenti achromians): a neurocutaneous syndrome. J Pediatr. 1977;90:236-240.
-
(1977)
J Pediatr
, vol.90
, pp. 236-240
-
-
Schwartz, M.F.1
Esterly, N.B.2
Fretzin, D.F.3
Pergament, E.4
Rozenfeld, I.H.5
-
22
-
-
0023932022
-
Hypomelanosis of Ito: Neurological complications in 34 cases
-
Pascual-Castroviejo I, Lopez-Rodriguez L, de la Cruz Medina M, Salamanca-Maesso C, Herrero CR. Hypomelanosis of Ito: neurological complications in 34 cases. Can J Neurol Sci. 1988;15:124-129.
-
(1988)
Can J Neurol Sci
, vol.15
, pp. 124-129
-
-
Pascual-Castroviejo, I.1
Lopez-Rodriguez, L.2
De la Cruz Medina, M.3
Salamanca-Maesso, C.4
Herrero, C.R.5
-
23
-
-
0026528367
-
Hypomelanosis of Ito diagnostic criteria and report of 41 cases
-
Ruiz-Maldonado R, Toussaint S, Tamayo L, Laterza A, del Castillo V. Hypomelanosis of Ito diagnostic criteria and report of 41 cases. Pediatr Dermatol. 1992;9:1-10.
-
(1992)
Pediatr Dermatol
, vol.9
, pp. 1-10
-
-
Ruiz-Maldonado, R.1
Toussaint, S.2
Tamayo, L.3
Laterza, A.4
Del Castillo, V.5
-
24
-
-
0027418618
-
The association of hemifacial microsomia, homolateral micro/anophthalmos, hemihypotrophy, dental anomalies, submucous cleft palate, CNS malformations and hypopigmented skin lesions following Blaschko's lines in two unrelated female patients: Further evidence for a lethal mutation surviving in mosaic form in 'hypomelanosis of Ito.'
-
Fryns JP, Lemaire J, Timmermans J, Soekarman D, Van den Berghe H. The association of hemifacial microsomia, homolateral micro/anophthalmos, hemihypotrophy, dental anomalies, submucous cleft palate, CNS malformations and hypopigmented skin lesions following Blaschko's lines in two unrelated female patients: further evidence for a lethal mutation surviving in mosaic form in 'hypomelanosis of Ito.' Genet Couns. 1993;4:63-67.
-
(1993)
Genet Couns
, vol.4
, pp. 63-67
-
-
Fryns, J.P.1
Lemaire, J.2
Timmermans, J.3
Soekarman, D.4
Van den Berghe, H.5
-
25
-
-
0027203993
-
Hypomelanosis of Ito associated with mosaicism for trisomy 7 and apparent 'pseudomosaicism' at amniocentesis
-
Jenkins D, Martin K, Young ID. Hypomelanosis of Ito associated with mosaicism for trisomy 7 and apparent 'pseudomosaicism' at amniocentesis. J Med Genet. 1993;30:783-784.
-
(1993)
J Med Genet
, vol.30
, pp. 783-784
-
-
Jenkins, D.1
Martin, K.2
Young, I.D.3
-
26
-
-
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;25:809-818.
-
(1988)
J Med Genet
, vol.25
, pp. 809-818
-
-
Donnai, D.1
Read, A.P.2
McKeown, C.3
Andrews, T.4
-
27
-
-
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. Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito. J Pediatr. 1990;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
-
29
-
-
0023546478
-
Reticulate hyperpigmentation distributed in a zosteriform fashion: A new clinical type of hyperpigmentation
-
Iijima S, Naito Y, Naito S, Uyeno K. Reticulate hyperpigmentation distributed in a zosteriform fashion: a new clinical type of hyperpigmentation. Br J Dermatol. 1987;117:503-510.
-
(1987)
Br J Dermatol
, vol.117
, pp. 503-510
-
-
Iijima, S.1
Naito, Y.2
Naito, S.3
Uyeno, K.4
-
30
-
-
0025832535
-
Reticulate hyperpigmentation of Iijima, Naito, and Uyeno: A European case
-
Bjorngren H, Holst R. Reticulate hyperpigmentation of Iijima, Naito, and Uyeno: a European case. Acta Dermatol Venereol (Stockh). 1991;71:248-250.
-
(1991)
Acta Dermatol Venereol (Stockh)
, vol.71
, pp. 248-250
-
-
Bjorngren, H.1
Holst, R.2
-
31
-
-
0027269386
-
Linear and whorled nevoid hypermelanosis
-
Kanwar AJ. Linear and whorled nevoid hypermelanosis. Int J Dermatol. 1993; 32:385-386.
-
(1993)
Int J Dermatol
, vol.32
, pp. 385-386
-
-
Kanwar, A.J.1
-
33
-
-
0028242643
-
Familial linear and whorled nevoid hypermelanosis
-
Akiyama M, Aranami A, Sasaki Y, Ebihara T, Sugiura M. Familial linear and whorled nevoid hypermelanosis. J Am Acad Dermatol. 1994;30:831-833.
-
(1994)
J Am Acad Dermatol
, vol.30
, pp. 831-833
-
-
Akiyama, M.1
Aranami, A.2
Sasaki, Y.3
Ebihara, T.4
Sugiura, M.5
-
34
-
-
0018101892
-
Zosteriform lentiginous naevus with ipsilateral rigid cavus foot
-
Port M, Courniotes J, Podwal M. Zosteriform lentiginous naevus with ipsilateral rigid cavus foot. Br J Dermatol. 1978;98:693-698.
-
(1978)
Br J Dermatol
, vol.98
, pp. 693-698
-
-
Port, M.1
Courniotes, J.2
Podwal, M.3
-
35
-
-
0018650482
-
Zebra-like hyperpigmentation in an infant with multiple congenital defects
-
Alimurung FM, Lapenas D, Willis I, Lang P. Zebra-like hyperpigmentation in an infant with multiple congenital defects. Arch Dermatol. 1979;115:878-881.
-
(1979)
Arch Dermatol
, vol.115
, pp. 878-881
-
-
Alimurung, F.M.1
Lapenas, D.2
Willis, I.3
Lang, P.4
-
36
-
-
0026589422
-
Linear and whorled nevoid hypermelanosis in a child with chromosomal mosaicism
-
Kubota Y, Shimura Y. Linear and whorled nevoid hypermelanosis in a child with chromosomal mosaicism. Int J Dermatol. 1992;31:345-347.
-
(1992)
Int J Dermatol
, vol.31
, pp. 345-347
-
-
Kubota, Y.1
Shimura, Y.2
-
37
-
-
0027156771
-
Three patients with ring (X) chromosomes and a severe phenotype
-
Dennis NR, Collins AL, Crolla JA, Cockwell AE, Fisher AM, Jacobs PA. Three patients with ring (X) chromosomes and a severe phenotype. J Med Genet. 1993;30:482-486.
-
(1993)
J Med Genet
, vol.30
, pp. 482-486
-
-
Dennis, N.R.1
Collins, A.L.2
Crolla, J.A.3
Cockwell, A.E.4
Fisher, A.M.5
Jacobs, P.A.6
-
38
-
-
0028094709
-
Asymmetry and skin pigmentary anomalies in chromosome mosaicism
-
Woods CG, Bankier A, Curry J, et al. Asymmetry and skin pigmentary anomalies in chromosome mosaicism. J Med Genet. 1994;31:694-701.
-
(1994)
J Med Genet
, vol.31
, pp. 694-701
-
-
Woods, C.G.1
Bankier, A.2
Curry, J.3
-
41
-
-
0017986554
-
Infant with abnormal pigmentation, malformations, and immune deficiency
-
Ment L, Alper J, Sirota RL, Holmes LB. Infant with abnormal pigmentation, malformations, and immune deficiency. Arch Dermatol. 1978;114:1043-1044.
-
(1978)
Arch Dermatol
, vol.114
, pp. 1043-1044
-
-
Ment, L.1
Alper, J.2
Sirota, R.L.3
Holmes, L.B.4
-
42
-
-
0027209623
-
Triple structure mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation
-
Bocian E, Mazurczak T, Bulawa E, Stanczak H, Rowicka G. Triple structure mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation. J Med Genet. 1993;30:614-615.
-
(1993)
J Med Genet
, vol.30
, pp. 614-615
-
-
Bocian, E.1
Mazurczak, T.2
Bulawa, E.3
Stanczak, H.4
Rowicka, G.5
-
44
-
-
0011163138
-
Congenital and genetic disorders associated with hypopigmentation
-
Orlow SJ. Congenital and genetic disorders associated with hypopigmentation. Curr Probl Dermatol. 1994;6:157-184.
-
(1994)
Curr Probl Dermatol
, vol.6
, pp. 157-184
-
-
Orlow, S.J.1
-
45
-
-
0014577786
-
Two unusual neurocutaneous disorders with facial cutaneous signs
-
Sugarman GI, Reed WB. Two unusual neurocutaneous disorders with facial cutaneous signs. Arch Neurol. 1969;21:242-247.
-
(1969)
Arch Neurol
, vol.21
, pp. 242-247
-
-
Sugarman, G.I.1
Reed, W.B.2
-
47
-
-
0027163670
-
Nevus depigmentosus in India: Experience with 50 patients
-
Dhar S, Kanwar AJ, Kaur S. Nevus depigmentosus in India: experience with 50 patients Pediatr Dermatol. 1993;10:299-300.
-
(1993)
Pediatr Dermatol
, vol.10
, pp. 299-300
-
-
Dhar, S.1
Kanwar, A.J.2
Kaur, S.3
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