-
1
-
-
33750984056
-
Case of hypertrophy of the gums
-
Gross S D. Case of hypertrophy of the gums. Louis-Ville Rev, 1: 232-237, 1856.
-
(1856)
Louis-Ville Rev
, vol.1
, pp. 232-237
-
-
Gross, S.D.1
-
2
-
-
0027917799
-
Julia Pastrand, the non descript: An example of congenital, generalized hypertrichosis terminalis with gingival hyperplasia
-
Bondenson J, Miles AEW. Julia Pastrand, the non descript: an example of congenital, generalized hypertrichosis terminalis with gingival hyperplasia. Am J Med Genet, 47: 198-212, 1993.
-
(1993)
Am J Med Genet
, vol.47
, pp. 198-212
-
-
Bondenson, J.1
Miles, A.E.W.2
-
3
-
-
0016252799
-
Hypertrichosis with hereditary gingival hyperplasia
-
Winter G, Simpkiss M. hypertrichosis with hereditary gingival hyperplasia. Arch Dis Child, 49: 394-399, 1974.
-
(1974)
Arch Dis Child
, vol.49
, pp. 394-399
-
-
Winter, G.1
Simpkiss, M.2
-
4
-
-
0029055927
-
Child hood hypertrichosis, diagnosis and management
-
Baumeister FAM, Schwarz HP, Stengel-Rutkowsky S. child hood hypertrichosis, diagnosis and management. Arch Dis Child, 72: 457-459, 1995.
-
(1995)
Arch Dis Child
, vol.72
, pp. 457-459
-
-
Baumeister, F.A.M.1
Schwarz, H.P.2
Stengel-Rutkowsky, S.3
-
5
-
-
0015068755
-
Heterogeneity in gingival fibromatosis birth defects
-
Williams and Wilkins, Baltimore
-
Witkop, C.J. heterogeneity in gingival fibromatosis birth defects. original actual series. vol 7, part II, Williams and Wilkins, Baltimore; 210, 1971.
-
(1971)
Original Actual Series
, vol.7
, Issue.PART II
, pp. 210
-
-
Witkop, C.J.1
-
6
-
-
0027504043
-
Ambras syndrome: Delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion(8)(p11.2;q22)
-
Baumeister FAM, Egger J, Schildhauer MT, Stengel-Rutkowski S. Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion(8)(p11.2;q22). Clin Genet, 44: 121-128, 1993.
-
(1993)
Clin Genet
, vol.44
, pp. 121-128
-
-
Baumeister, F.A.M.1
Egger, J.2
Schildhauer, M.T.3
Stengel-Rutkowski, S.4
-
7
-
-
0028125215
-
Ambras syndrome and congenital generalized hypertrichosis
-
Cantu J, Figuera L. Ambras syndrome and congenital generalized hypertrichosis. Clin Genet, 46: 384, 1994.
-
(1994)
Clin Genet
, vol.46
, pp. 384
-
-
Cantu, J.1
Figuera, L.2
-
8
-
-
0028577612
-
Differentiation of congenital hypertrichosis from Ambras Syndrome
-
Baumeister FAM, Stengel-Rutkowsky S. differentiation of congenital hypertrichosis from Ambras Syndrome Clin Genet, 46: 441, 1994.
-
(1994)
Clin Genet
, vol.46
, pp. 441
-
-
Baumeister, F.A.M.1
Stengel-Rutkowsky, S.2
-
9
-
-
0020052574
-
A distinct osteochondrodysplasia with hypertrichosis individualization of a probable autosomal recessive entity
-
Cantu JM, Garcia-Cruz D, Sanchez-Corona J, Hernandez A, Nazara Z. A distinct osteochondrodysplasia with hypertrichosis individualization of a probable autosomal recessive entity Hum Genet, 60: 36-41, 1982.
-
(1982)
Hum Genet
, vol.60
, pp. 36-41
-
-
Cantu, J.M.1
Garcia-Cruz, D.2
Sanchez-Corona, J.3
Hernandez, A.4
Nazara, Z.5
-
10
-
-
0031048676
-
Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Further delineation of a new genetic syndrome
-
Garcia-Cruz D, Sanchez-Corona J, Nazara Z et al. Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome. Am J Med Genet 69: 138-151, 1997.
-
(1997)
Am J Med Genet
, vol.69
, pp. 138-151
-
-
Garcia-Cruz, D.1
Sanchez-Corona, J.2
Nazara, Z.3
-
11
-
-
12244266443
-
Hypertrichosis terminalis, gingival hyperplasia and a characteristic face: A new dictinct entity
-
Canun S et al. hypertrichosis terminalis, gingival hyperplasia and a characteristic face:a new dictinct entity. Am J Med Genet, 116A: 278-283, 2003.
-
(2003)
Am J Med Genet
, vol.116 A
, pp. 278-283
-
-
Canun, S.1
-
12
-
-
0014691933
-
Hereditary gingival fibromatosis
-
Anderson J, Cunliffe WJ, Roberts DF, and Close H. Hereditary gingival fibromatosis. British Medical Journal, 3: 218, 1969.
-
(1969)
British Medical Journal
, vol.3
, pp. 218
-
-
Anderson, J.1
Cunliffe, W.J.2
Roberts, D.F.3
Close, H.4
-
13
-
-
79959446197
-
The hair
-
In: Ebling FJG, Drawleer R, Rook A, eds. 4th ed. Oxford:Blackwell, 1986:1959.
-
Rook A, Wilkinson DS, Ebling FJG, Champion RM, Burttan JL. The hair In: Ebling FJG, Drawleer R, Rook A, eds. Textbook of Dermatology, 4th ed. Oxford:Blackwell
-
(1959)
Textbook of Dermatology
, vol.1986
-
-
Rook, A.1
Wilkinson, D.S.2
Ebling, F.J.G.3
Champion, R.M.4
Burttan, J.L.5
-
14
-
-
0006146609
-
Hair
-
Fitz Patrick TB, Eisen AZ, Wolff K, Freedberg IM, Austen KF, eds. 3rd ed. Newyork: Mc Grow-Hill
-
Bertollins AT, Freedbery IM. Hair In: Fitz Patrick TB, Eisen AZ, Wolff K, Freedberg IM, Austen KF, eds. Dermatology in general medicine, 3rd ed. Newyork: Mc Grow-Hill: 645-646, 1987.
-
(1987)
Dermatology in General Medicine
, pp. 645-646
-
-
Bertollins, A.T.1
Freedbery, I.M.2
-
15
-
-
0021321227
-
A new form of hypertrichosis inherited as an x linked dominant trait
-
Mocias-Floias MA, Garcia Cruz D, Rivera H, Escobar-Lujan M, Melendez Vega A, Rivas Campos D, Rodiquez-Collazo F, Moreno-Arellano I, Cantu JM. A new form of hypertrichosis inherited as an x linked dominant trait. Hum Genet, 66: 66-70, 1984.
-
(1984)
Hum Genet
, vol.66
, pp. 66-70
-
-
Mocias-Floias, M.A.1
Garcia Cruz, D.2
Rivera, H.3
Escobar-Lujan, M.4
Melendez Vega, A.5
Rivas Campos, D.6
Rodiquez-Collazo, F.7
Moreno-Arellano, I.8
Cantu, J.M.9
-
17
-
-
0023909391
-
Hereditary generalized gingival fibromatosis associated with hypertrichosis
-
Carnero RC Bornancini CA. Hereditary generalized gingival fibromatosis associated with hypertrichosis. J Oral Maxillofacial Surg, 46: 415-520, 1988.
-
(1988)
J Oral Maxillofacial Surg
, vol.46
, pp. 415-520
-
-
Carnero, R.C.1
Bornancini, C.A.2
-
18
-
-
0024312174
-
Idiopathic familial gingival fibromatosis associated with mental retardation, epilepcy and hypertrichosis
-
Anavi Y, jerman P, Mintz S, Kiviti S. Idiopathic familial gingival fibromatosis associated with mental retardation, epilepcy and hypertrichosis. Dev. Med Child Neural, 31: 538-542, 1989.
-
(1989)
Dev. Med Child Neural
, vol.31
, pp. 538-542
-
-
Anavi, Y.1
Jerman, P.2
Mintz, S.3
Kiviti, S.4
-
19
-
-
0025296136
-
Gingival fibromatosis, mental retardation, epilepcy, and hypertrichosis
-
Kiss P. gingival fibromatosis, mental retardation, epilepcy, and hypertrichosis. Dev(Med) Child Neural, 32: 459-460, 1990.
-
(1990)
Dev(Med) Child Neural
, vol.32
, pp. 459-460
-
-
Kiss, P.1
-
20
-
-
0016193707
-
Variation in inheritance and expression of gingival fibromatosis
-
Jorgenson RJ, Cocker ME, variation in inheritance and expression of gingival fibromatosis. J Periodontol, 45: 472, 1974.
-
(1974)
J Periodontol
, vol.45
, pp. 472
-
-
Jorgenson, R.J.1
Cocker, M.E.2
-
21
-
-
66749111309
-
Copy-number mutations on chromosome17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia
-
Sun M, Li N, Dong W, Chen Z, Liu Q, Xu Y et al. Copy-number mutations on chromosome17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia. Am J Hum Genet, 84: 807-813, 2009.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 807-813
-
-
Sun, M.1
Li, N.2
Dong, W.3
Chen, Z.4
Liu, Q.5
Xu, Y.6
-
22
-
-
0014684580
-
Hypertrichosis portrayed in art
-
1969
-
Ravin JG, Hodge GP 1969. Hypertrichosis portrayed in art. JAMA, 207: 533-53522, 1969.
-
(1969)
JAMA
, vol.207
, pp. 533-53522
-
-
Ravin, J.G.1
Hodge, G.P.2
-
23
-
-
0017202168
-
Hypertrichosis lanuginose in a mother and son
-
Freire-Maria, Felizali J., de Figuereid AC, Opitz JM, Parreira M, Maia NA. Hypertrichosis lanuginose in a mother and son. Clin Genet, 10: 303-306, 1976.
-
(1976)
Clin Genet
, vol.10
, pp. 303-306
-
-
Freire-Maria, F.J.1
De Figuereid, A.C.2
Opitz, J.M.3
Parreira, M.4
Maia, N.A.5
-
24
-
-
0031848683
-
A new case of Ambras syndrome associated with a paracentric inversion (8)(q12;q22)
-
Balducci R, Toscano V, Tedeschi B, Mangiantini A, Toscano R., Galasso C., Cianfacani S., Boscherini B. A new case of Ambras syndrome associated with a paracentric inversion (8)(q12;q22) Clin Genet, 53: 466-468, 1998.
-
(1998)
Clin Genet
, vol.53
, pp. 466-468
-
-
Balducci, R.1
Toscano, V.2
Tedeschi, B.3
Mangiantini, A.4
Toscano, R.5
Galasso, C.6
Cianfacani, S.7
Boscherini, B.8
-
25
-
-
0029808815
-
An autosomal dominant syndrome of acromegaloid facial appearance and generalized hypertrichosis terminalis
-
Irvin DA, Dolan MO, Hadden DR, Stewart FJ, Bingham EA, Nevin NC. An autosomal dominant syndrome of acromegaloid facial appearance and generalized hypertrichosis terminalis, J.Med Genet, 33: 972-974, 1996.
-
(1996)
J.Med Genet
, vol.33
, pp. 972-974
-
-
Irvin, D.A.1
Dolan, M.O.2
Hadden, D.R.3
Stewart, F.J.4
Bingham, E.A.5
Nevin, N.C.6
-
26
-
-
33750984056
-
Case of hypertrophy of the gums
-
Gross S D. Case of hypertrophy of the gums. Louis-Ville Rev, 1: 232-237, 1856.
-
(1856)
Louis-Ville Rev
, vol.1
, pp. 232-237
-
-
Gross, S.D.1
|