-
1
-
-
0034213642
-
Syndrome de Feingold
-
Alessandri JL et al. Syndrome de Feingold. Arch Pediatr 2000; 7: 637-640
-
(2000)
Arch Pediatr
, vol.7
, pp. 637-640
-
-
Alessandri, J.L.1
-
2
-
-
0014775994
-
Familial duodenal atresia
-
Berant M, Kahana D. Familial duodenal atresia. Arch Dis Child 1970; 45: 281-282
-
(1970)
Arch Dis Child
, vol.45
, pp. 281-282
-
-
Berant, M.1
Kahana, D.2
-
3
-
-
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. 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 1991; 28: 389-394
-
(1991)
J Med Genet
, vol.28
, pp. 389-394
-
-
Brunner, H.G.1
Winter, R.M.2
-
4
-
-
0033928260
-
Familial syndromic esophageal atresia maps to 2 p23-p24
-
Celli J et al. Familial syndromic esophageal atresia maps to 2 p23-p24. Am J Hum Genet 2000; 66: 436-444
-
(2000)
Am J Hum Genet
, vol.66
, pp. 436-444
-
-
Celli, J.1
-
5
-
-
0027052344
-
VATER/VACTERL association: Clinical variability and expanding phenotype including laryngeal stenosis
-
Corsello G et al. VATER/VACTERL association: clinical variability and expanding phenotype including laryngeal stenosis. Am J Med Genet 1992; 44: 813-815
-
(1992)
Am J Med Genet
, vol.44
, pp. 813-815
-
-
Corsello, G.1
-
6
-
-
0030725244
-
Feingold syndrome: Report of a new family and review
-
Courtens W et al. Feingold syndrome: report of a new family and review. Am J Med Genet 1997; 73: 55-60
-
(1997)
Am J Med Genet
, vol.73
, pp. 55-60
-
-
Courtens, W.1
-
7
-
-
0025343079
-
Fryns syndrome: An autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia
-
Cunniff C et al. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia. Pediatrics 1990; 85: 499-504
-
(1990)
Pediatrics
, vol.85
, pp. 499-504
-
-
Cunniff, C.1
-
8
-
-
0003593937
-
Case report 30
-
Feingold M. Case report 30. Synd Ident 1975; 3: 16-17
-
(1975)
Synd Ident
, vol.3
, pp. 16-17
-
-
Feingold, M.1
-
9
-
-
0031002838
-
Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay
-
Feingold M et al. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. Am J Med Genet 1997; 69: 245-249
-
(1997)
Am J Med Genet
, vol.69
, pp. 245-249
-
-
Feingold, M.1
-
10
-
-
0030843742
-
MODED: Microcephaly-oculo-digito-esophageal-duodenal syndrome
-
Frydman M et al. MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome. Am J Med Genet 1997; 71: 251-257
-
(1997)
Am J Med Genet
, vol.71
, pp. 251-257
-
-
Frydman, M.1
-
11
-
-
0015028898
-
Duodenal atresia in the newborn
-
Gourevitch A. Duodenal atresia in the newborn. Ann R Coll Surg Engl 1971; 48: 141-158
-
(1971)
Ann R Coll Surg Engl
, vol.48
, pp. 141-158
-
-
Gourevitch, A.1
-
12
-
-
0029007429
-
Familial intestinal polyatresia syndrome
-
Gungor N et al. Familial intestinal polyatresia syndrome. Clin Genet 1995; 47: 245-247
-
(1995)
Clin Genet
, vol.47
, pp. 245-247
-
-
Gungor, N.1
-
13
-
-
0013692119
-
Tracheoesophageal fistula/esophageal atresia multiple congenital anomaly syndrome: Feingold type
-
Hall BD. Tracheoesophageal fistula/esophageal atresia multiple congenital anomaly syndrome: Feingold type. Proc Greenwood Genet Center 1993; 13: 123-124
-
(1993)
Proc Greenwood Genet Center
, vol.13
, pp. 123-124
-
-
Hall, B.D.1
-
14
-
-
0025736434
-
Association of annular pancreas and duodenal obstruction - Evidence for Mendelian inheritance?
-
Hendricks SK, Sybert VP. Association of annular pancreas and duodenal obstruction - evidence for Mendelian inheritance? Clin Genet 1991; 39: 383-385
-
(1991)
Clin Genet
, vol.39
, pp. 383-385
-
-
Hendricks, S.K.1
Sybert, V.P.2
-
15
-
-
0030738131
-
Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies
-
Innis JW et al. Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies. Am J Med Genet 1997; 71: 150-155
-
(1997)
Am J Med Genet
, vol.71
, pp. 150-155
-
-
Innis, J.W.1
-
16
-
-
0025042565
-
Microcephaly, mesobrachyphalangy, and tracheoesophageal fistula: MMT syndrome
-
König R et al. Microcephaly, mesobrachyphalangy, and tracheoesophageal fistula: MMT syndrome. Dysm Clin Genet 1990; 4: 83-86
-
(1990)
Dysm Clin Genet
, vol.4
, pp. 83-86
-
-
König, R.1
-
17
-
-
0026775847
-
New syndrome? Tracheoesophageal fistula, gastrointestinal abnormalities, hypospadias, and prenatal growth deficiency
-
Martinez-Frias M-L et al. New syndrome? Tracheoesophageal fistula, gastrointestinal abnormalities, hypospadias, and prenatal growth deficiency. Am J Med Genet 1992; 44: 352-355
-
(1992)
Am J Med Genet
, vol.44
, pp. 352-355
-
-
Martinez-Frias, M.-L.1
-
18
-
-
0034129807
-
Vertebral anomalies in a new family with ODED syndrome
-
Piersall LD et al. Vertebral anomalies in a new family with ODED syndrome. Clin Genet 2000; 57: 444-448
-
(2000)
Clin Genet
, vol.57
, pp. 444-448
-
-
Piersall, L.D.1
-
19
-
-
0023200826
-
Familial apple peel jejunal atresia
-
Seashore JH et al. Familial apple peel jejunal atresia. Pediatrics 1987; 80: 540-544
-
(1987)
Pediatrics
, vol.80
, pp. 540-544
-
-
Seashore, J.H.1
-
20
-
-
0030443298
-
Further evidence for a syndrome of "apple peel" intestinal atresia, ocular anomalies and microcephaly
-
Slee J, Goldblatt J. Further evidence for a syndrome of "apple peel" intestinal atresia, ocular anomalies and microcephaly. Clin Genet 1996; 50: 260-262
-
(1996)
Clin Genet
, vol.50
, pp. 260-262
-
-
Slee, J.1
Goldblatt, J.2
-
21
-
-
0032486113
-
Anomalies in Down syndrome individuals in a large population-based registry
-
Torfs CP, Christianson RE. Anomalies in Down syndrome individuals in a large population-based registry. Am J Med Genet 1998; 77: 431-438
-
(1998)
Am J Med Genet
, vol.77
, pp. 431-438
-
-
Torfs, C.P.1
Christianson, R.E.2
|