-
1
-
-
0023279764
-
Congenital microgastria: Case report and review of the literature
-
Aintablian NH, Slim MS, Antoun BW (1987). Congenital microgastria: Case report and review of the literature. Pediatr Surg Internat 2:307-310.
-
(1987)
Pediatr Surg Internat
, vol.2
, pp. 307-310
-
-
Aintablian, N.H.1
Slim, M.S.2
Antoun, B.W.3
-
2
-
-
0021080223
-
Treatment of congenital microgastria and dumping syndrome
-
Anderson KD, Guzzetta PC (1983). Treatment of congenital microgastria and dumping syndrome. J Pediatr Surg 18:747-750.
-
(1983)
J Pediatr Surg
, vol.18
, pp. 747-750
-
-
Anderson, K.D.1
Guzzetta, P.C.2
-
3
-
-
0017977515
-
Hypoglycemie et microgastrie
-
Choulot JT (1978). Hypoglycemie et microgastrie. Arch Frans Pediatr 35:651-655.
-
(1978)
Arch Frans Pediatr
, vol.35
, pp. 651-655
-
-
Choulot, J.T.1
-
5
-
-
0027953334
-
VACTERL with hydrocephalus: A further case with probable autosomal recessive inheritance
-
Corsello G, Giuffre L (1994). VACTERL with hydrocephalus: A further case with probable autosomal recessive inheritance. Am J Med Genet 49:137-138.
-
(1994)
Am J Med Genet
, vol.49
, pp. 137-138
-
-
Corsello, G.1
Giuffre, L.2
-
6
-
-
0027251850
-
Congenital microgastria and limb reduction defects
-
Cunniff C, Williamson-Kruse L, Olney AH (1993). Congenital microgastria and limb reduction defects. Pediatrics 91:1192-1194.
-
(1993)
Pediatrics
, vol.91
, pp. 1192-1194
-
-
Cunniff, C.1
Williamson-Kruse, L.2
Olney, A.H.3
-
9
-
-
8044243592
-
Congenital microgastria, growth hormone deficiency and diabetes insipidus
-
Hernaiz Driever P, Gohlich-Ratman G, Konig R, Heller K, Schmidt H, Baum RP, Bohles HJ (1997). Congenital microgastria, growth hormone deficiency and diabetes insipidus. Eur J Pediatr 156:37-40.
-
(1997)
Eur J Pediatr
, vol.156
, pp. 37-40
-
-
Hernaiz Driever, P.1
Gohlich-Ratman, G.2
Konig, R.3
Heller, K.4
Schmidt, H.5
Baum, R.P.6
Bohles, H.J.7
-
11
-
-
0031749320
-
Congenital microgastria: A case report and review of literature
-
Kroes EJ, Festen C (1998). Congenital microgastria: a case report and review of literature. Pediat Surg Int 13:416-418.
-
(1998)
Pediat Surg Int
, vol.13
, pp. 416-418
-
-
Kroes, E.J.1
Festen, C.2
-
12
-
-
0028905401
-
'Microgastria-limb reduction' complex with congenital heart disease and twinning
-
Lurie IW, Magee CA, Sun CCJ, Ferencz C (1995). 'Microgastria-limb reduction' complex with congenital heart disease and twinning. Clin Dysmorphol 4:150-155.
-
(1995)
Clin Dysmorphol
, vol.4
, pp. 150-155
-
-
Lurie, I.W.1
Magee, C.A.2
Sun, C.C.J.3
Ferencz, C.4
-
13
-
-
0024332795
-
Congenital microgastria and hypoplastic upper limb anomalies
-
Leuder GT, Fitz-James A, Dowton SB (1989). Congenital microgastria and hypoplastic upper limb anomalies. Am J Med Genet 32:368-370.
-
(1989)
Am J Med Genet
, vol.32
, pp. 368-370
-
-
Leuder, G.T.1
Fitz-James, A.2
Dowton, S.B.3
-
15
-
-
0026435061
-
Microgastria-hypoplastic upper limb association: A severe expression including microphthalmia, single nostril and arhinencephaly
-
Meinecke P, Bönnemann CG, Laas R (1992). Microgastria-hypoplastic upper limb association: A severe expression including microphthalmia, single nostril and arhinencephaly. Clin Dysmorphol 1:43-46.
-
(1992)
Clin Dysmorphol
, vol.1
, pp. 43-46
-
-
Meinecke, P.1
Bönnemann, C.G.2
Laas, R.3
-
16
-
-
0026742503
-
VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies?
-
Porteous MEM, Cross I, Burn J (1992). VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies? Am J Med Genet 43:1032-1034.
-
(1992)
Am J Med Genet
, vol.43
, pp. 1032-1034
-
-
Porteous, M.E.M.1
Cross, I.2
Burn, J.3
-
18
-
-
8044223093
-
Hemmungsbildung des Magens, Mangel der Milz und des Netzes
-
Robert HLF (1842). Hemmungsbildung des Magens, Mangel der Milz und des Netzes. Arch Anat Physiol Wissenschaft Med:57-60.
-
(1842)
Arch Anat Physiol Wissenschaft Med
, vol.57
, pp. 60
-
-
Robert, H.L.F.1
-
19
-
-
0026095047
-
Laryngotracheoesophageal cleft (type IV): Management and repair of lesions beyond the carina
-
Ryan DP, Muehrcke DD, Doody DP, Kim SH, Donahoe PK (1991). Laryngotracheoesophageal cleft (type IV): management and repair of lesions beyond the carina. J Pediatr Surg 26:962-970.
-
(1991)
J Pediatr Surg
, vol.26
, pp. 962-970
-
-
Ryan, D.P.1
Muehrcke, D.D.2
Doody, D.P.3
Kim, S.H.4
Donahoe, P.K.5
-
20
-
-
0015071277
-
Kongenitale Mikrogastrie in Verbindung mit Skelettmissbildungen-ein neues Syndrom
-
Schulz RD, Niemann F (1971). Kongenitale Mikrogastrie in Verbindung mit Skelettmissbildungen-ein neues Syndrom. Helv Paediatr Acta 26:185-191.
-
(1971)
Helv Paediatr Acta
, vol.26
, pp. 185-191
-
-
Schulz, R.D.1
Niemann, F.2
-
21
-
-
0027429752
-
Microgastria-case report and a review of the literature
-
Tanaka K, Tsuchida Y, Hashizume K, Kawarasaki H, Suglyama M (1993). Microgastria-case report and a review of the literature. Eur J Pediatr Surg 3:290-292.
-
(1993)
Eur J Pediatr Surg
, vol.3
, pp. 290-292
-
-
Tanaka, K.1
Tsuchida, Y.2
Hashizume, K.3
Kawarasaki, H.4
Suglyama, M.5
-
23
-
-
0028847882
-
Syndromal hypothalamic hamartoblastoma with holoprosencephaly sequence, microphthalmia, pulmonary malformation, radial hypoplasia and Müllerian regression: Further delineation of new syndrome?
-
Verloes A, Narcey F, Fallet-Bianco C (1995). Syndromal hypothalamic hamartoblastoma with holoprosencephaly sequence, microphthalmia, pulmonary malformation, radial hypoplasia and Müllerian regression: Further delineation of new syndrome? Clin Dysmorphol 4:33-37.
-
(1995)
Clin Dysmorphol
, vol.4
, pp. 33-37
-
-
Verloes, A.1
Narcey, F.2
Fallet-Bianco, C.3
-
24
-
-
0027166367
-
VACTERL with hydrocephalus: Spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance
-
Wang H, Hunter AGW, Clifford B, Mclaughlin M, Thompson D (1993). VACTERL with hydrocephalus: Spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance. Am J Med Genet 47:114-117.
-
(1993)
Am J Med Genet
, vol.47
, pp. 114-117
-
-
Wang, H.1
Hunter, A.G.W.2
Clifford, B.3
McLaughlin, M.4
Thompson, D.5
|