-
1
-
-
0025834804
-
Robin sequence with facial and digital anomalies in two half-brothers by the same mother
-
Chitayat D., Meunier C.M., Hodgkinson K.A., Azouz M.E.: Robin sequence with facial and digital anomalies in two half-brothers by the same mother. Am. J. Med. Genet., 1991, 40, 167-172.
-
(1991)
Am. J. Med. Genet.
, vol.40
, pp. 167-172
-
-
Chitayat, D.1
Meunier, C.M.2
Hodgkinson, K.A.3
Azouz, M.E.4
-
2
-
-
0022369313
-
Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
-
Filippi G.: Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome? Am. J. Med. Genet., 1985, 22, 821-824.
-
(1985)
Am. J. Med. Genet.
, vol.22
, pp. 821-824
-
-
Filippi, G.1
-
3
-
-
0030021991
-
Filippi syndrome with mild learning difficulties
-
Fryer A.: Filippi syndrome with mild learning difficulties. Clin. Dysmorphol., 1996, 5, 35-39.
-
(1996)
Clin. Dysmorphol.
, vol.5
, pp. 35-39
-
-
Fryer, A.1
-
4
-
-
0029146202
-
Filippi syndrome: A new case with skeletal abnormalities
-
Héron D., Billette De Villemeur T., Munnich A., Lyonnet S.: Filippi syndrome: a new case with skeletal abnormalities. J. Med. Genet., 1995, 32, 659-661.
-
(1995)
J. Med. Genet.
, vol.32
, pp. 659-661
-
-
Héron, D.1
Billette De Villemeur, T.2
Munnich, A.3
Lyonnet, S.4
-
5
-
-
0027511392
-
Microcephaly and digital anomalies: A newly recognized syndrome of recessively inherited mental retardation
-
Kelly T.E., Kirson L., Wyatt J.: Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation. Am. J. Med. Genet., 1993, 45, 353-355.
-
(1993)
Am. J. Med. Genet.
, vol.45
, pp. 353-355
-
-
Kelly, T.E.1
Kirson, L.2
Wyatt, J.3
-
6
-
-
0025083819
-
The craniodigital syndrome of Scott: Report of a second family
-
Lorenz P., Hinkel G.K., Hoffmann C., Ruppreght E.: The craniodigital syndrome of Scott: report of a second family. Am. J. Med. Genet., 1990, 37, 224-226.
-
(1990)
Am. J. Med. Genet.
, vol.37
, pp. 224-226
-
-
Lorenz, P.1
Hinkel, G.K.2
Hoffmann, C.3
Ruppreght, E.4
-
7
-
-
0027207605
-
Short stature, microcephaly, characteristic face, syndactyly and mental retardation: The Filippi syndrome. Report on a second family
-
Meinecke P.: Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family. Genet. Couns., 1993, 4, 147-151.
-
(1993)
Genet. Couns.
, vol.4
, pp. 147-151
-
-
Meinecke, P.1
-
8
-
-
0030867501
-
An additional case of craniodigital syndrome: Variable expression of the Filippi syndrome?
-
Orrico A., Hayek G.: An additional case of craniodigital syndrome: variable expression of the Filippi syndrome? Clin. Genet., 1997, 52, 177-179.
-
(1997)
Clin. Genet.
, vol.52
, pp. 177-179
-
-
Orrico, A.1
Hayek, G.2
-
9
-
-
0015044351
-
A new craniodigital syndrome with mental retardation
-
Scott C.R., Bryant J.I., Graham C.B.: A new craniodigital syndrome with mental retardation. J. Pediatr., 1971, 78, 658-663.
-
(1971)
J. Pediatr.
, vol.78
, pp. 658-663
-
-
Scott, C.R.1
Bryant, J.I.2
Graham, C.B.3
-
10
-
-
0030794875
-
On the nosology of the craniodigital syndromes: Report of a family and review of the literature
-
Soekarman D., Volcke PH., Fryns J.P.: On the nosology of the craniodigital syndromes: report of a family and review of the literature. Genet. Couns., 1997, 8, 217-222.
-
(1997)
Genet. Couns.
, vol.8
, pp. 217-222
-
-
Soekarman, D.1
Volcke, P.H.2
Fryns, J.P.3
-
11
-
-
0028897567
-
Craniodigital syndromes: Report of a child with Filippi syndrome and discussion of differential diagnosis
-
Toriello H.V., Higgins J.V.: Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis. Am. J. Med. Genet., 1995, 55, 200-204.
-
(1995)
Am. J. Med. Genet.
, vol.55
, pp. 200-204
-
-
Toriello, H.V.1
Higgins, J.V.2
-
12
-
-
0032747648
-
Expanding the phenotype of Filippi syndrome: A report of three cases
-
Walpole I.R., Parry T., Goldblatt J.: Expanding the phenotype of Filippi syndrome: a report of three cases. Clin. Dysmorphol., 1999, 8, 235-240.
-
(1999)
Clin. Dysmorphol.
, vol.8
, pp. 235-240
-
-
Walpole, I.R.1
Parry, T.2
Goldblatt, J.3
-
13
-
-
0032707124
-
Filippi syndrome: Report of three additional cases
-
Williams M.S., Williams J.L., Wargowski D.S., Pauli R.M., Pletcher B.A.: Filippi syndrome: report of three additional cases. Am. J. Med. Genet., 1999, 87, 128-133.
-
(1999)
Am. J. Med. Genet.
, vol.87
, pp. 128-133
-
-
Williams, M.S.1
Williams, J.L.2
Wargowski, D.S.3
Pauli, R.M.4
Pletcher, B.A.5
-
14
-
-
0026695720
-
Three sibs with phalangeal anomalies, microcephaly, severe mental retardation, and neurological abnormalities
-
Woods C.G., Crouchman M., Huson S.M.: Three sibs with phalangeal anomalies, microcephaly, severe mental retardation, and neurological abnormalities. J. Med. Genet., 1992, 29, 500-502.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 500-502
-
-
Woods, C.G.1
Crouchman, M.2
Huson, S.M.3
-
15
-
-
0026573939
-
Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation: A new syndrome?
-
Zerres K., Rietschel M., Rietschel E., Majewski F., Meinecke P.: Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation: a new syndrome? J. Med. Genet., 1992, 29, 269-271.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 269-271
-
-
Zerres, K.1
Rietschel, M.2
Rietschel, E.3
Majewski, F.4
Meinecke, P.5
|