-
1
-
-
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, Cianfarani S, Boscherini B. 1998. A new case of Ambras syndrome associated with a paracentric inversion (8)(q12;q22). Clin Genet 53:466-468.
-
(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
Cianfarani, S.7
Boscherini, B.8
-
2
-
-
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. 1993. 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)
Clin Genet
, vol.44
, pp. 121-128
-
-
Baumeister, F.A.M.1
Egger, J.2
Schildhauer, M.T.3
Stengel-Rutkowski, S.4
-
3
-
-
0014807539
-
Congenital hypertrichosis lanuginose
-
Beighton P. 1970. Congenital hypertrichosis lanuginose. Arch Dermatol 101:669-672.
-
(1970)
Arch Dermatol
, vol.101
, pp. 669-672
-
-
Beighton, P.1
-
4
-
-
0027917799
-
Julia Pastrana, the nondescript: An example of congenital, generalized hypertrichosis terminals with gingival hyperplasia
-
Bondeson J, Miles AEW. 1993. Julia Pastrana, the nondescript: an example of congenital, generalized hypertrichosis terminals with gingival hyperplasia. Am J Med Genet 47:198-212.
-
(1993)
Am J Med Genet
, vol.47
, pp. 198-212
-
-
Bondeson, J.1
Miles, A.E.W.2
-
5
-
-
0020052574
-
A distinct osteochondrodysplasia with hypertrichosis-individualization of a probable autosomal recessive entity
-
Cantú JM, García-Cruz D, Sánchez-Corona J, Hernández A, Nazara Z. 1982. A distinct osteochondrodysplasia with hypertrichosis-individualization of a probable autosomal recessive entity. Hum Genet 60:36-41.
-
(1982)
Hum Genet
, vol.60
, pp. 36-41
-
-
Cantú, J.M.1
García-Cruz, D.2
Sánchez-Corona, J.3
Hernández, A.4
Nazara, Z.5
-
6
-
-
0017202168
-
Hypertrichosis lanuginose in a mother and son
-
Freire-Maia N, Felizali J, de Figuereido AC, Opitz JM, Parreira M, Maia NA. 1976. Hypertrichosis lanuginose in a mother and son. Clin Genet 10:303-306.
-
(1976)
Clin Genet
, vol.10
, pp. 303-306
-
-
Freire-Maia, N.1
Felizali, J.2
De Figuereido, A.C.3
Opitz, J.M.4
Parreira, M.5
Maia, N.A.6
-
7
-
-
0031048676
-
Congenital hypertrichosis, ostechondrodysplasia, and cardiomegaly: Further delineation of a new genetic syndrome
-
García-Cruz D, Sánchez-Corona J, Nazará Z, García-Cruz MO, Figuera LE, Castañeda V, Cantú JM. 1997. Congenital hypertrichosis, ostechondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome. Am J Med Genet 69:138-151.
-
(1997)
Am J Med Genet
, vol.69
, pp. 138-151
-
-
García-Cruz, D.1
Sánchez-Corona, J.2
Nazará, Z.3
García-Cruz, M.O.4
Figuera, L.E.5
Castañeda, V.6
Cantú, J.M.7
-
8
-
-
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. 1996. An autosomal dominant syndrome of acromegaloid facial appearance and generalized hypertrichosis terminalis. J Med Genet 33:972-974.
-
(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
-
9
-
-
0021321227
-
A new form of hypertrichosis inherited as an X-linked dominant trait
-
Macías-Flores MA, García-Cruz D, Rivera H, Escobar-Lujan M, Meléndez-Vega A, Rivas-Campos D, Rodríguez-Collazo F, Moreno-Arellano I, Cantú JM. 1984. A new form of hypertrichosis inherited as an X-linked dominant trait. Hum Genet 66:66-70.
-
(1984)
Hum Genet
, vol.66
, pp. 66-70
-
-
Macías-Flores, M.A.1
García-Cruz, D.2
Rivera, H.3
Escobar-Lujan, M.4
Meléndez-Vega, A.5
Rivas-Campos, D.6
Rodríguez-Collazo, F.7
Moreno-Arellano, I.8
Cantú, J.M.9
-
10
-
-
33646214960
-
-
McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD)
-
Online Mendelian Inheritance in Man (OMIM) (TM). 2000. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD). World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/
-
(2000)
-
-
-
11
-
-
0016598013
-
Somatometría pediátrica. Estudio semilongitudinal en niños de la Ciudad de México
-
Ramos-Galván R. 1975. Somatometría pediátrica. Estudio semilongitudinal en niños de la Ciudad de México. Arch Inv Med (Mex) 6(Suppl 1):83-396.
-
(1975)
Arch Inv Med (Mex)
, vol.6
, Issue.SUPPL. 1
, pp. 83-396
-
-
Ramos-Galván, R.1
-
12
-
-
0014684580
-
Hypertrichosis portrayed in art
-
Ravin JG, Hodge GP. 1969. Hypertrichosis portrayed in art. JAMA 207:533-535.
-
(1969)
JAMA
, vol.207
, pp. 533-535
-
-
Ravin, J.G.1
Hodge, G.P.2
-
13
-
-
0016252799
-
Hypertrichosis with hereditary gingival hyperplasia
-
Winter GB, Simpkiss MJ. 1974. Hypertrichosis with hereditary gingival hyperplasia. Arch Dis Child 49:394-399.
-
(1974)
Arch Dis Child
, vol.49
, pp. 394-399
-
-
Winter, G.B.1
Simpkiss, M.J.2
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