-
2
-
-
0015884563
-
The lacrimo-auriculo-dental-digital syndrome
-
Hollister DW, Klein SH, De Jager HJ, Lachmann RS, Rimoin DL. The lacrimo-auriculo-dental-digital syndrome. J Paediatr. 1973;83:438-444.
-
(1973)
J Paediatr
, vol.83
, pp. 438-444
-
-
Hollister, D.W.1
Klein, S.H.2
De Jager, H.J.3
Lachmann, R.S.4
Rimoin, D.L.5
-
3
-
-
0014082974
-
Mesoectodermal dysplasia: A new combination of abnormalities
-
Levy WJ. Mesoectodermal dysplasia: a new combination of abnormalities. Am J Ophthalmol. 1969; 63:978-982.
-
(1969)
Am J Ophthalmol
, vol.63
, pp. 978-982
-
-
Levy, W.J.1
-
4
-
-
0014399820
-
Familial microtia with meatal atresia in two sibships
-
Ellwood LC, Winter ST, Dar H. Familial microtia with meatal atresia in two sibships. J Med Genet. 1968;5:289-291.
-
(1968)
J Med Genet
, vol.5
, pp. 289-291
-
-
Ellwood, L.C.1
Winter, S.T.2
Dar, H.3
-
6
-
-
0014489279
-
Conductive hearing loss and malformed low set ears as a possible recessive syndrome
-
Mengel MC, Koningsmark BW, Berlin CI, McKusick VA. Conductive hearing loss and malformed low set ears as a possible recessive syndrome. J Med Genet. 1969;6:14-21.
-
(1969)
J Med Genet
, vol.6
, pp. 14-21
-
-
Mengel, M.C.1
Koningsmark, B.W.2
Berlin, C.I.3
McKusick, V.A.4
-
8
-
-
0025836623
-
Congenital conductive or mixed deafness, pre-auricular sinus, external ear anomaly, commissural lip pits: An autosomal dominant inherited syndrome
-
Marres HAM, Cremers CWRJ. Congenital conductive or mixed deafness, pre-auricular sinus, external ear anomaly, commissural lip pits: an autosomal dominant inherited syndrome. Ann Otol Rhinol Laryngol. 1991;100:928-932.
-
(1991)
Ann Otol Rhinol Laryngol
, vol.100
, pp. 928-932
-
-
Marres, H.A.M.1
Cremers, C.W.R.J.2
-
9
-
-
0025063276
-
EEC syndrome: Report on 20 new patients, clinical and genetic considerations
-
Rodini ESO, Richieri-Costa A. EEC syndrome: report on 20 new patients, clinical and genetic considerations. Am J Med Genet. 1990;37:42-53.
-
(1990)
Am J Med Genet
, vol.37
, pp. 42-53
-
-
Rodini, E.S.O.1
Richieri-Costa, A.2
-
10
-
-
0018950468
-
The IVIC syndrome: A new autosomal dominant complex pleiotropic syndrome with radial ray hypoplasia, hearing impairment, external ophthalmoplegia and thrombocytopenia
-
Arias S, Penchaszadeh VB, Pinto-Cisternas J, Larrauri S. The IVIC syndrome: a new autosomal dominant complex pleiotropic syndrome with radial ray hypoplasia, hearing impairment, external ophthalmoplegia and thrombocytopenia. Am J Med Genet. 1980;6:25-59.
-
(1980)
Am J Med Genet
, vol.6
, pp. 25-59
-
-
Arias, S.1
Penchaszadeh, V.B.2
Pinto-Cisternas, J.3
Larrauri, S.4
-
11
-
-
0017683776
-
The lacrimo-auriculodento-digital syndrome
-
Shiang EL, Holmes LB. The lacrimo-auriculodento-digital syndrome. Pediatrics. 1977;59:927-930.
-
(1977)
Pediatrics
, vol.59
, pp. 927-930
-
-
Shiang, E.L.1
Holmes, L.B.2
-
12
-
-
0022591768
-
LADD syndrome: Report of new cases and review of the clinical spectrum
-
Wiedemann HR, Drechser J. LADD syndrome: report of new cases and review of the clinical spectrum. Eur J Pediatr. 1986;144:579-582.
-
(1986)
Eur J Pediatr
, vol.144
, pp. 579-582
-
-
Wiedemann, H.R.1
Drechser, J.2
-
13
-
-
0021995034
-
Phenotypic variation in the LADD syndrome
-
Thompson E, Pembry M, Graham J. Phenotypic variation in the LADD syndrome. J Med Genet. 1985;22:382-385.
-
(1985)
J Med Genet
, vol.22
, pp. 382-385
-
-
Thompson, E.1
Pembry, M.2
Graham, J.3
-
14
-
-
0029970946
-
Ossicular reconstruction in cases of absent or inadequate incus, congenital malformations of the middle ear and epitympanic fixation of the incus and malleus
-
Tange RA. Ossicular reconstruction in cases of absent or inadequate incus, congenital malformations of the middle ear and epitympanic fixation of the incus and malleus. ORL J Otorhinolaryngol Relat Spec. 1996;58:143-146.
-
(1996)
ORL J Otorhinolaryngol Relat Spec
, vol.58
, pp. 143-146
-
-
Tange, R.A.1
|