-
1
-
-
0031750402
-
Lethal autosomal recessive syndrome with intrauterine growth retardation, intra and extrahepatic biliary atresia, and esophageal and duodenal atresia
-
Anneren G, Meurling S, Lilja H, Wallander J, von Dobeln U (1998). Lethal autosomal recessive syndrome with intrauterine growth retardation, intra and extrahepatic biliary atresia, and esophageal and duodenal atresia. Am J Med Genet 78:306-307.
-
(1998)
Am J Med Genet
, vol.78
, pp. 306-307
-
-
Anneren, G.1
Meurling, S.2
Lilja, H.3
Wallander, J.4
Von Dobeln, U.5
-
2
-
-
0031045069
-
Biliary atresia: Should all patients undergo a portoenterostomy?
-
Azarow KS, Phillips MJ, Sandler AD, Hagerstrand I, Superina RA (1997). Biliary atresia: should all patients undergo a portoenterostomy? J Pediatr Surg 32:168-172.
-
(1997)
J Pediatr Surg
, vol.32
, pp. 168-172
-
-
Azarow, K.S.1
Phillips, M.J.2
Sandler, A.D.3
Hagerstrand, I.4
Superina, R.A.5
-
3
-
-
0035079885
-
Mandibulo dysosotosis, microcephaly and thorax deformities in two brothers: A new recessive syndrome?
-
Delb W, Lipfert S, Henn W (2001). Mandibulo dysosotosis, microcephaly and thorax deformities in two brothers: a new recessive syndrome? Clin Dysmorphol 10:105-109.
-
(2001)
Clin Dysmorphol
, vol.10
, pp. 105-109
-
-
Delb, W.1
Lipfert, S.2
Henn, W.3
-
4
-
-
18244397461
-
Acrofacial dysostosis type Rodriguez
-
Dimitrov B, Balikova I, Jekova N, Vakrilova L, Fryns JP, Simeonov E (2005). Acrofacial dysostosis type Rodriguez. Am J Med Genet 135:81-85.
-
(2005)
Am J Med Genet
, vol.135
, pp. 81-85
-
-
Dimitrov, B.1
Balikova, I.2
Jekova, N.3
Vakrilova, L.4
Fryns, J.P.5
Simeonov, E.6
-
6
-
-
0033851255
-
Duodenal atresia, biliary atresia, and intestinal infarct in truncal aplasia cutis congenital
-
Lane W, Zanol K (2000). Duodenal atresia, biliary atresia, and intestinal infarct in truncal aplasia cutis congenital. Pediatr Dermatol 4:290-292.
-
(2000)
Pediatr Dermatol
, vol.4
, pp. 290-292
-
-
Lane, W.1
Zanol, K.2
-
7
-
-
0029909795
-
A familial disorder with duodenal atresia and tetralogy of Fallot
-
Lemire EG, Evans JA, Giddins NG, Harman CR, Wiseman NE, Chudley AE (1996). A familial disorder with duodenal atresia and tetralogy of Fallot. Am J Med Genet 66:39-44.
-
(1996)
Am J Med Genet
, vol.66
, pp. 39-44
-
-
Lemire, E.G.1
Evans, J.A.2
Giddins, N.G.3
Harman, C.R.4
Wiseman, N.E.5
Chudley, A.E.6
-
8
-
-
0026775847
-
Tracheoesophageal fistula, gastrointestinal abnormalities, hypospadias, and prenatal growth deficiency
-
Martinez-Frias ML, Frias JL, Galan E, Domingo R, Paisan L, Blanco M (1992). Tracheoesophageal fistula, gastrointestinal abnormalities, hypospadias, and prenatal growth deficiency. Am J Med Genet 44:352-355.
-
(1992)
Am J Med Genet
, vol.44
, pp. 352-355
-
-
Martinez-Frias, M.L.1
Frias, J.L.2
Galan, E.3
Domingo, R.4
Paisan, L.5
Blanco, M.6
-
10
-
-
0027452302
-
Acrofacial dysostoses: Review and report of a previously undescribed condition
-
Opitz JM, Molica F, Sorge G, Milana G, Cimino G, Caltabiano M (1993). Acrofacial dysostoses: review and report of a previously undescribed condition. Am J Med Genet 47:660-678.
-
(1993)
Am J Med Genet
, vol.47
, pp. 660-678
-
-
Opitz, J.M.1
Molica, F.2
Sorge, G.3
Milana, G.4
Cimino, G.5
Caltabiano, M.6
-
11
-
-
0026573551
-
Acrofacial dysosotosis syndrome type Rodriguez. A new lethal MCA syndrome
-
Petit P, Moerman P, Fryns JP (1992). Acrofacial dysosotosis syndrome type Rodriguez. A new lethal MCA syndrome. Am J Med Genet 42:342-345.
-
(1992)
Am J Med Genet
, vol.42
, pp. 342-345
-
-
Petit, P.1
Moerman, P.2
Fryns, J.P.3
-
13
-
-
0027450343
-
Cleft lip and palate, scoliosis, skeletal and cardiac malformations and other dysmorphic features in a child. Case report
-
Stromme P, Knudtzon J, Westvik J, Traaholt L, Brandt-Hansen P (1993). Cleft lip and palate, scoliosis, skeletal and cardiac malformations and other dysmorphic features in a child. Case report. Scand J Pl Rec Surg 27:71-74.
-
(1993)
Scand J Pl Rec Surg
, vol.27
, pp. 71-74
-
-
Stromme, P.1
Knudtzon, J.2
Westvik, J.3
Traaholt, L.4
Brandt-Hansen, P.5
-
14
-
-
0031567205
-
Patterson-Stevenson-Fotaine syndrome: 30 Year follow-up and clinical details of a further affected case
-
Wilkie AOM, Goodacre TEE (1997). Patterson-Stevenson-Fotaine syndrome: 30 year follow-up and clinical details of a further affected case. Am J Med Genet 69:433-434.
-
(1997)
Am J Med Genet
, vol.69
, pp. 433-434
-
-
Wilkie, A.O.M.1
Goodacre, T.E.E.2
-
15
-
-
19244373803
-
Townes-Brocks and Pendred syndrome in the same patient
-
Yano S, Watanabe Y, Yoshino M, Aida K, Kato H (1998). Townes-Brocks and Pendred syndrome in the same patient. Am J Med Genet 77:330-331.
-
(1998)
Am J Med Genet
, vol.77
, pp. 330-331
-
-
Yano, S.1
Watanabe, Y.2
Yoshino, M.3
Aida, K.4
Kato, H.5
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