-
1
-
-
0024515683
-
Fryns syndrome: Report on 8 new cases
-
Ayrné S, Julian C, Gabarelli D, Mariotti B, Luciani A, Sudan N, Maurin N, Philip N, Serville F, Carles D, Rolland M, Girand F. 1989. Fryns syndrome: Report on 8 new cases. Clin Genet 35:191-201.
-
(1989)
Clin Genet
, vol.35
, pp. 191-201
-
-
Ayrné, S.1
Julian, C.2
Gabarelli, D.3
Mariotti, B.4
Luciani, A.5
Sudan, N.6
Maurin, N.7
Philip, N.8
Serville, F.9
Carles, D.10
Rolland, M.11
Girand, F.12
-
2
-
-
0024494910
-
Congenital diapragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome
-
Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG. 1989. Congenital diapragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome. Am J Med Genet 32:93-99.
-
(1989)
Am J Med Genet
, vol.32
, pp. 93-99
-
-
Bamforth, J.S.1
Leonard, C.O.2
Chodirker, B.N.3
Chitayat, D.4
Gritter, H.L.5
Evans, J.A.6
Keena, B.7
Pantzar, T.8
Friedman, J.M.9
Hall, J.G.10
-
3
-
-
0028789524
-
Fryns syndrome: Two further cases without lateral diaphragmatic defects
-
Bartsch O, Meinecke P, Kamin G. 1995. Fryns syndrome: Two further cases without lateral diaphragmatic defects. Clin Dysmorphol 4:352-358.
-
(1995)
Clin Dysmorphol
, vol.4
, pp. 352-358
-
-
Bartsch, O.1
Meinecke, P.2
Kamin, G.3
-
4
-
-
0344117759
-
Pulmonary agenesis, microphthalmia, and diaphragmatic defect: New syndrome or association?
-
Berkenstadt M, Lev D, Achiron R, Rosner M, Barkai G. 1999. Pulmonary agenesis, microphthalmia, and diaphragmatic defect: New syndrome or association? Am J Med Genet 86:6-8.
-
(1999)
Am J Med Genet
, vol.86
, pp. 6-8
-
-
Berkenstadt, M.1
Lev, D.2
Achiron, R.3
Rosner, M.4
Barkai, G.5
-
5
-
-
0025343079
-
Fryns syndrome: An autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia
-
Cunniff C, Jones KL, Saal HM, Stern HJ. 1990. Fryns syndrome: An autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia. Pediatrics 85:499-504.
-
(1990)
Pediatrics
, vol.85
, pp. 499-504
-
-
Cunniff, C.1
Jones, K.L.2
Saal, H.M.3
Stern, H.J.4
-
6
-
-
0025936706
-
Apparent Fryns syndrome and aneuploidy: Evidence for a disturbance of the midline developmental field
-
Dean JCS, Couzin DA, Gray ES, Lloyd DJ, Stephen GS. 1991. Apparent Fryns syndrome and aneuploidy: Evidence for a disturbance of the midline developmental field. Clin Genet 40:349-352.
-
(1991)
Clin Genet
, vol.40
, pp. 349-352
-
-
Dean, J.C.S.1
Couzin, D.A.2
Gray, E.S.3
Lloyd, D.J.4
Stephen, G.S.5
-
7
-
-
0024364857
-
Ring chromosome 15 in a patient with features of Fryns' syndrome
-
deJong G, Rossouw RA, Retief AE. 1989. Ring chromosome 15 in a patient with features of Fryns' syndrome. J Med Genet 26:469-472.
-
(1989)
J Med Genet
, vol.26
, pp. 469-472
-
-
DeJong, G.1
Rossouw, R.A.2
Retief, A.E.3
-
8
-
-
0027361847
-
Antenatal detection of congenital diaphragmatic hernias: The Northern region experience
-
Dillon E, Renwick M. 1993. Antenatal detection of congenital diaphragmatic hernias: The Northern region experience. Clin Radiol 48:264-267.
-
(1993)
Clin Radiol
, vol.48
, pp. 264-267
-
-
Dillon, E.1
Renwick, M.2
-
9
-
-
0032875542
-
Hematometra and sudden death after status epilepticus in an adolescent female with Fryns syndrome
-
Dingens M, Fryns JP. 1999. Hematometra and sudden death after status epilepticus in an adolescent female with Fryns syndrome. Genet Couns 10:329-330.
-
(1999)
Genet Couns
, vol.10
, pp. 329-330
-
-
Dingens, M.1
Fryns, J.P.2
-
10
-
-
0018123910
-
Absent left hemidiaphragm, arhinencephaly, and cardiac malformation
-
Fitch N, Srolovitz H, Robitaille Y, Guttman F. 1978. Absent left hemidiaphragm, arhinencephaly, and cardiac malformation. J Med Genet 15:399-401.
-
(1978)
J Med Genet
, vol.15
, pp. 399-401
-
-
Fitch, N.1
Srolovitz, H.2
Robitaille, Y.3
Guttman, F.4
-
11
-
-
0023202062
-
Fryns syndrome: A variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia
-
Fryns JP. 1987. Fryns syndrome: A variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia. J Med Genet 24:271-274.
-
(1987)
J Med Genet
, vol.24
, pp. 271-274
-
-
Fryns, J.P.1
-
12
-
-
0031748601
-
Scalp defects in Fryns syndrome
-
Fryns JP. 1998. Scalp defects in Fryns syndrome. Genet Couns 9:153-154.
-
(1998)
Genet Couns
, vol.9
, pp. 153-154
-
-
Fryns, J.P.1
-
13
-
-
0018305302
-
A new lethal syndrome with cloudy corneae, diaphragmatic defects, and distal limb deformities
-
Fryns JP, Moerman F, Goddeeris P, Bossuyt C, Van Den Berghe H. 1979. A new lethal syndrome with cloudy corneae, diaphragmatic defects, and distal limb deformities. Hum Genet 50:65-70.
-
(1979)
Hum Genet
, vol.50
, pp. 65-70
-
-
Fryns, J.P.1
Moerman, F.2
Goddeeris, P.3
Bossuyt, C.4
Van Den Berghe, H.5
-
14
-
-
33646219575
-
A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies: The Fryns syndrome
-
Fryns JP, Moerman P, Van den Berghe H, Aymé S. 1989. A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies: The Fryns syndrome. J Génét Hum 37:207-205.
-
(1989)
J Génét Hum
, vol.37
, pp. 207-205
-
-
Fryns, J.P.1
Moerman, P.2
Van den Berghe, H.3
Aymé, S.4
-
15
-
-
0027938902
-
Prenatal diagnosis and long survival of Fryns syndrome
-
Gadow EC, Lippold S, Serafin E, Salgado LJ, Garcia C, Prudent L. 1994. Prenatal diagnosis and long survival of Fryns syndrome. Prenat Diagn 13:673-676.
-
(1994)
Prenat Diagn
, vol.13
, pp. 673-676
-
-
Gadow, E.C.1
Lippold, S.2
Serafin, E.3
Salgado, L.J.4
Garcia, C.5
Prudent, L.6
-
16
-
-
0019223582
-
Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities: A new lethal syndrome
-
Goddeeris P, Fryns J, Van Den Berghe H. 1980. Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities: A new lethal syndrome. J Genet Human 28:57-60, 1980.
-
(1980)
J Genet Human
, vol.28
, pp. 57-60
-
-
Goddeeris, P.1
Fryns, J.2
Van Den Berghe, H.3
-
18
-
-
0025376405
-
Terminal deletion of 6q and Fryns syndrome: A microdeletion/syndrome pair?
-
Krassikoff N, Sekhon GS. 1990. Terminal deletion of 6q and Fryns syndrome: A microdeletion/syndrome pair? (Letter) Am J Med Genet 36:363-364.
-
(1990)
Am J Med Genet
, vol.36
, pp. 363-364
-
-
Krassikoff, N.1
Sekhon, G.S.2
-
20
-
-
0028024115
-
Fryns syndrome: A rare familial cause of congenital diaphragmatic hernia
-
Langer JC, Winthrop AL, Whelan D. 1994. Fryns syndrome: A rare familial cause of congenital diaphragmatic hernia. J Ped Surg 29:1266-1267.
-
(1994)
J Ped Surg
, vol.29
, pp. 1266-1267
-
-
Langer, J.C.1
Winthrop, A.L.2
Whelan, D.3
-
21
-
-
0020596403
-
Fryns syndrome: A new variable multiple congenital anomaly (MCA) syndrome
-
Lubinsky M, Severn C, Rapoport JM. 1983. Fryns syndrome: A new variable multiple congenital anomaly (MCA) syndrome. Am J Med Genet 14:461-466.
-
(1983)
Am J Med Genet
, vol.14
, pp. 461-466
-
-
Lubinsky, M.1
Severn, C.2
Rapoport, J.M.3
-
23
-
-
0022369562
-
The Fryns syndrome: Diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance
-
Meinecke P, Fryns JP. 1985. The Fryns syndrome: Diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance. Clin Genet 28:516-520.
-
(1985)
Clin Genet
, vol.28
, pp. 516-520
-
-
Meinecke, P.1
Fryns, J.P.2
-
24
-
-
0024269679
-
The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): Report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome
-
Moerman P, Fryns JP, Vandenberghe K, Devlieger H, Lauweryns JM. 1988. The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): Report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome. Am J Med Genet 31:805-814.
-
(1988)
Am J Med Genet
, vol.31
, pp. 805-814
-
-
Moerman, P.1
Fryns, J.P.2
Vandenberghe, K.3
Devlieger, H.4
Lauweryns, J.M.5
-
25
-
-
0026537970
-
Prenatal diagnosis of Fryns syndrome
-
Pellissier MC, Philip N, Potier A, Scheiner C, Aymé S, Mattéi JF, Giraud F. 1992. Prenatal diagnosis of Fryns syndrome. Prenat Diag 12:299-303.
-
(1992)
Prenat Diag
, vol.12
, pp. 299-303
-
-
Pellissier, M.C.1
Philip, N.2
Potier, A.3
Scheiner, C.4
Aymé, S.5
Mattéi, J.F.6
Giraud, F.7
-
26
-
-
0025773348
-
Elode,op;pgoca; stidu pf cpmgemota; dophragmatic defects with special references to aeitiology
-
Philip N, Gambarelli D, Guys JM, Cambouviles J, Aymé S. 1991. E[ode,op;pgoca; stidu pf cpmgemota; dophragmatic defects with special references to aeitiology. Eur J Pediatr 150:726-729.
-
(1991)
Eur J Pediatr
, vol.150
, pp. 726-729
-
-
Philip, N.1
Gambarelli, D.2
Guys, J.M.3
Cambouviles, J.4
Aymé, S.5
-
28
-
-
0034684716
-
Variability in the phenotypic expression of Fryns syndrome: A report of two sibships
-
Ramsing M, Gillessen-Kaesbach G, Holzgreve W, Fritz B, Rehder H. 2000. Variability in the phenotypic expression of Fryns syndrome: A report of two sibships. Am J Med Genet 95:415-424.
-
(2000)
Am J Med Genet
, vol.95
, pp. 415-424
-
-
Ramsing, M.1
Gillessen-Kaesbach, G.2
Holzgreve, W.3
Fritz, B.4
Rehder, H.5
-
29
-
-
0028099179
-
Lethal Pallisterillian syndrome: Phenotypic similarity with Fryns syndrome
-
Rodriguèz JI, Garcia I, Álvarez J, Delicádo A, Palácios J. 1994. Lethal Pallisterillian syndrome: Phenotypic similarity with Fryns syndrome. Am J Med Genet 53(2):176-181.
-
(1994)
Am J Med Genet
, vol.53
, Issue.2
, pp. 176-181
-
-
Rodriguèz, J.I.1
Garcia, I.2
Álvarez, J.3
Delicádo, A.4
Palácios, J.5
-
31
-
-
0032167521
-
Fryns syndrome: Prenatal diagnosis and pathologic correlation
-
Sheffield JS, Twickler DM, Timmons C, Land K, Harrod M, Ramus RM. 1998. Fryns syndrome: Prenatal diagnosis and pathologic correlation. J Uttrasound Med 17:585-589.
-
(1998)
J Uttrasound Med
, vol.17
, pp. 585-589
-
-
Sheffield, J.S.1
Twickler, D.M.2
Timmons, C.3
Land, K.4
Harrod, M.5
Ramus, R.M.6
-
32
-
-
0028792594
-
Fryns syndrome survivors and neurologic outcome
-
Van Hove JLK, Spiridigliozzi GA, Heinz R, McConkie-Rosell A, Iafolla K, Kahler SG. 1995. Fryns syndrome survivors and neurologic outcome. Am J Med Genet 59:334-340.
-
(1995)
Am J Med Genet
, vol.59
, pp. 334-340
-
-
Van Hove, J.L.K.1
Spiridigliozzi, G.A.2
Heinz, R.3
McConkie-Rosell, A.4
Iafolla, K.5
Kahler, S.G.6
-
33
-
-
0034605366
-
Discordant phenotype in monozygotic twins with Fryns syndrome
-
Vargas JE, Cos GF, Korf BR. 2000. Discordant phenotype in monozygotic twins with Fryns syndrome. Am J Med Genet 94:42-45.
-
(2000)
Am J Med Genet
, vol.94
, pp. 42-45
-
-
Vargas, J.E.1
Cos, G.F.2
Korf, B.R.3
-
35
-
-
0025990654
-
Fryns syndrom without diagphragmatic hernia?
-
Willems PJ, Keersmaekers GHA, Dom KE, Colpaert C, Schatteman E, Gergote IBP, Dumon JE. 1991. Fryns syndrom without diagphragmatic hernia? Am J Med Genet 41:255-257.
-
(1991)
Am J Med Genet
, vol.41
, pp. 255-257
-
-
Willems, P.J.1
Keersmaekers, G.H.A.2
Dom, K.E.3
Colpaert, C.4
Schatteman, E.5
Gergote, I.B.P.6
Dumon, J.E.7
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