-
1
-
-
0002070475
-
On brachydactyly and symphalangism
-
Bell J (1951): On brachydactyly and symphalangism. Treasury Hum Inherit 5:1-30.
-
(1951)
Treasury Hum Inherit
, vol.5
, pp. 1-30
-
-
Bell, J.1
-
2
-
-
0025797367
-
Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia
-
Brunner HG, Winter RM (1991): Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia. J Med Genet 28:389-394.
-
(1991)
J Med Genet
, vol.28
, pp. 389-394
-
-
Brunner, H.G.1
Winter, R.M.2
-
3
-
-
0003593937
-
Case report 30
-
Feingold M (1975): Case report 30. Synd Ident 3:16-17.
-
(1975)
Synd Ident
, vol.3
, pp. 16-17
-
-
Feingold, M.1
-
4
-
-
0017838162
-
An unusual microcephaly
-
Feingold M (1978): An unusual microcephaly. Hosp Pract 13:44, 49.
-
(1978)
Hosp Pract
, vol.13
, pp. 44
-
-
Feingold, M.1
-
5
-
-
0022369313
-
Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly
-
Filippi G (1985): Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome? Am J Med Genet 22:821-824.
-
(1985)
A New Syndrome? Am J Med Genet
, vol.22
, pp. 821-824
-
-
Filippi, G.1
-
6
-
-
0018409706
-
Classification and identification of inherited brachydactylies
-
Fitch N (1979): Classification and identification of inherited brachydactylies. J Med Genet 16:36-44.
-
(1979)
J Med Genet
, vol.16
, pp. 36-44
-
-
Fitch, N.1
-
7
-
-
0027511392
-
Microcephaly and digital anomalies: A newly recognized syndrome of recessively inherited mental retardation
-
Kelly TE, Kirson L, Wyatt J (1993): Microcephaly and digital anomalies: A newly recognized syndrome of recessively inherited mental retardation. Am J Med Genet 45:353-355.
-
(1993)
Am J Med Genet
, vol.45
, pp. 353-355
-
-
Kelly, T.E.1
Kirson, L.2
Wyatt, J.3
-
8
-
-
0025042565
-
Microcephaly, mesobrachyphalangy, and tracheoesophagcal fistula: MMT syndrome
-
Konig R, Selzer G, Stolp A, Fuchs S (1990): Microcephaly, mesobrachyphalangy, and tracheoesophagcal fistula: MMT syndrome. Dysmorphol Clini Genet 4:83-86.
-
(1990)
Dysmorphol Clini Genet
, vol.4
, pp. 83-86
-
-
Konig, R.1
Selzer, G.2
Stolp, A.3
Fuchs, S.4
-
9
-
-
0027207605
-
Short stature, microcephaly, characteristic face, syndactyly and mental retardation: The Filippi syndrome report on a second family
-
Meinecke P (1993): Short stature, microcephaly, characteristic face, syndactyly and mental retardation: The Filippi syndrome report on a second family. Genet Counseling 4:147-151.
-
(1993)
Genet Counseling
, vol.4
, pp. 147-151
-
-
Meinecke, P.1
-
10
-
-
0025131567
-
Microcephaly: General considerations and aids to nosology
-
Opitz JM, Holt MC (1990): Microcephaly: General considerations and aids to nosology. J Craniofacial Genet Dev Biol 10:175-204.
-
(1990)
J Craniofacial Genet Dev Biol
, vol.10
, pp. 175-204
-
-
Opitz, J.M.1
Holt, M.C.2
-
11
-
-
0013656160
-
The genetics of hand malformations
-
Temtamy SA, McKusick VA (1978): The genetics of hand malformations. Birth Defects 14:1-619.
-
(1978)
Birth Defects
, vol.14
, pp. 1-619
-
-
Temtamy, S.A.1
McKusick, V.A.2
-
12
-
-
0028897567
-
Craniodigital syndromes: Report of a child with Filippi syndrome and discussion of differential diagnosis
-
Toriello HV, Higgins JV (1995): Craniodigital syndromes: Report of a child with Filippi syndrome and discussion of differential diagnosis. Am J Med Genet 55:200-204.
-
(1995)
Am J Med Genet
, vol.55
, pp. 200-204
-
-
Toriello, H.V.1
Higgins, J.V.2
-
13
-
-
0342862559
-
Hands and feet
-
Stevenson RE, Hall. JG. Goodman RM (eds): Oxford: Oxford University Press
-
Winter RM, Schroer RJ, Meyer LC (1993): Hands and feet. In Stevenson RE, Hall. JG. Goodman RM (eds): "Human Malformations and Related Anomalies," Vol. II. Oxford: Oxford University Press, pp 805-843.
-
(1993)
Human Malformations and Related Anomalies
, vol.2
, pp. 805-843
-
-
Winter, R.M.1
Schroer, R.J.2
Meyer, L.C.3
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