-
1
-
-
0020523606
-
Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family
-
Arnold GL, Bixler D, Girod D (1983): Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family. Am J Med Genet 16: 35-42.
-
(1983)
Am J Med Genet
, vol.16
, pp. 35-42
-
-
Arnold, G.L.1
Bixler, D.2
Girod, D.3
-
2
-
-
0001564443
-
The spleen
-
Stevenson RE, Hall JG, Goodman RM (eds): Oxford: Oxford Unviersity Press
-
Aylsworth AS (1993): The spleen. In: Stevenson RE, Hall JG, Goodman RM (eds): "Human malformations and related anomalies," 1st Edn. Oxford: Oxford Unviersity Press; pp. 307-317.
-
(1993)
"Human Malformations and Related Anomalies," 1st Edn.
, pp. 307-317
-
-
Aylsworth, A.S.1
-
3
-
-
0025017481
-
Diabetes mellitus during pregnancy and the risks for specific birth defects: A population based case-control study
-
Becerra JE, Khoury MJ, Cordero JF, Erickson JD (1990): Diabetes mellitus during pregnancy and the risks for specific birth defects: A population based case-control study. Pediatrics 85: 1-9.
-
(1990)
Pediatrics
, vol.85
, pp. 1-9
-
-
Becerra, J.E.1
Khoury, M.J.2
Cordero, J.F.3
Erickson, J.D.4
-
4
-
-
0029060788
-
Mutations of the connexin43 gap-junction gene in patients with heart malformations and defects of laterality
-
Britz-Cunningham SH, Shah MM, Zuppan CW, Fletcher WH (1995): Mutations of the connexin43 gap-junction gene in patients with heart malformations and defects of laterality. N Engl J Med 332: 1323-1329.
-
(1995)
N Engl J Med
, vol.332
, pp. 1323-1329
-
-
Britz-Cunningham, S.H.1
Shah, M.M.2
Zuppan, C.W.3
Fletcher, W.H.4
-
5
-
-
0026707667
-
Human situs determination is probably controlled by several different genes
-
Carmi R, Boughman JA, Rosenbaum KR (1992): Human situs determination is probably controlled by several different genes. Am J Med Genet 44: 246-247.
-
(1992)
Am J Med Genet
, vol.44
, pp. 246-247
-
-
Carmi, R.1
Boughman, J.A.2
Rosenbaum, K.R.3
-
6
-
-
0027454207
-
Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1
-
Casey B, Devoto M, Jones KL, Ballabio A (1993): Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1. Nat Genet 5: 403-407.
-
(1993)
Nat Genet
, vol.5
, pp. 403-407
-
-
Casey, B.1
Devoto, M.2
Jones, K.L.3
Ballabio, A.4
-
7
-
-
0020964067
-
Congenital anomalies among infants of diabetic mothers. Etiology, prevention, prenatal diagnosis
-
Cousins L (1983): Congenital anomalies among infants of diabetic mothers. Etiology, prevention, prenatal diagnosis. Am J Obstet Gynecol 147: 333-338.
-
(1983)
Am J Obstet Gynecol
, vol.147
, pp. 333-338
-
-
Cousins, L.1
-
8
-
-
0025269770
-
Maternal diabetes and cardiovascular malformations: Predominance of double outlet right ventricle and truncus arteriosus
-
Ferencz C, Rubin JD, McCarter RJ, Clark EB (1990): Maternal diabetes and cardiovascular malformations: predominance of double outlet right ventricle and truncus arteriosus. Teratology 41: 319-326.
-
(1990)
Teratology
, vol.41
, pp. 319-326
-
-
Ferencz, C.1
Rubin, J.D.2
McCarter, R.J.3
Clark, E.B.4
-
9
-
-
0015458911
-
The asplenia syndrome: A review of significant extracardiac structural abnormalities in 29 necropsied patients
-
Freedom RM (1972): The asplenia syndrome: A review of significant extracardiac structural abnormalities in 29 necropsied patients. J Pediatr 81: 1130-1133.
-
(1972)
J Pediatr
, vol.81
, pp. 1130-1133
-
-
Freedom, R.M.1
-
10
-
-
0017466987
-
Congenital malformations in infants of diabetic mothers
-
Gabbe SG (1977): Congenital malformations in infants of diabetic mothers. Obst Gynaecol Surv 32: 125-132.
-
(1977)
Obst Gynaecol Surv
, vol.32
, pp. 125-132
-
-
Gabbe, S.G.1
-
11
-
-
0024340830
-
Polyasplenia complex with mesocardia and renal agenesis in an infant of a diabetic mother
-
Gonzalez A, Krassikoff N, Gilbert-Barness EF (1989): Polyasplenia complex with mesocardia and renal agenesis in an infant of a diabetic mother. Am J Med Genet 32: 457-460.
-
(1989)
Am J Med Genet
, vol.32
, pp. 457-460
-
-
Gonzalez, A.1
Krassikoff, N.2
Gilbert-Barness, E.F.3
-
12
-
-
0003433343
-
Diabetes in pregnancy
-
Chalmers I, Enkin M, Keirse JNC (eds): Oxford: Oxford University Press
-
Hunter DJS (1989): Diabetes in pregnancy. In Chalmers I, Enkin M, Keirse JNC (eds): "Effective care in pregnancy and childbirth," 1st Edn, Oxford: Oxford University Press; pp. 578-593.
-
(1989)
"Effective Care in Pregnancy and Childbirth," 1st Edn
, pp. 578-593
-
-
Hunter, D.J.S.1
-
13
-
-
0024431357
-
Clinical-epidemiologic assessment of patterns of birth defects associated with human teratogens: Application to diabetic embryopathy
-
Khoury MJ, Becerra JE, Cordero JF, Erickson JD (1989): Clinical-epidemiologic assessment of patterns of birth defects associated with human teratogens: Application to diabetic embryopathy. Pediatrics 84: 658-665.
-
(1989)
Pediatrics
, vol.84
, pp. 658-665
-
-
Khoury, M.J.1
Becerra, J.E.2
Cordero, J.F.3
Erickson, J.D.4
-
14
-
-
0015112484
-
Rate and type of congenital anomalies among offspring of diabetic women
-
Kurcera J (1971): Rate and type of congenital anomalies among offspring of diabetic women. J Reprod Med 7: 61-70.
-
(1971)
J Reprod Med
, vol.7
, pp. 61-70
-
-
Kurcera, J.1
-
15
-
-
0017050268
-
Random determination of a developmental process. Reversal of normal visceral asymmetry in the mouse
-
Layton WM (1976): Random determination of a developmental process. Reversal of normal visceral asymmetry in the mouse. J Hered 67: 336-338.
-
(1976)
J Hered
, vol.67
, pp. 336-338
-
-
Layton, W.M.1
-
16
-
-
0024386521
-
Early pregnancy glycosylated hemoglobin, severity of diabetes, and fetal malformations
-
Lucas MJ, Leveno KJ, Williams ML, Raskin P, Whalley PJ (1989): Early pregnancy glycosylated hemoglobin, severity of diabetes, and fetal malformations. Am J Obstet Gynecol 161: 426-431.
-
(1989)
Am J Obstet Gynecol
, vol.161
, pp. 426-431
-
-
Lucas, M.J.1
Leveno, K.J.2
Williams, M.L.3
Raskin, P.4
Whalley, P.J.5
-
17
-
-
0023625914
-
X-linked laterality sequence: Situs inversus, complex cardiac defects, splenic defects
-
Mathias RS, Lacro RV, Lyons Jones K (1987): X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects. Am J Med Genet 28: 111-116.
-
(1987)
Am J Med Genet
, vol.28
, pp. 111-116
-
-
Mathias, R.S.1
Lacro, R.V.2
Lyons Jones, K.3
-
19
-
-
0018363182
-
Malformations in infants of diabetic mothers occur before the seventh gestational week
-
Mills JL, Baker L, Goldman AS (1979): Malformations in infants of diabetic mothers occur before the seventh gestational week. Diabetes 28: 292-293.
-
(1979)
Diabetes
, vol.28
, pp. 292-293
-
-
Mills, J.L.1
Baker, L.2
Goldman, A.S.3
-
20
-
-
0023841062
-
Lack of relation of increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis
-
Mills JL, Knopp RH, Simpson JL, Jovanovic-Peterson L, Metzger BE, Holmes LB, Aarons JH, Brown Z, Reed GF, Bieber FR, Van Allen M, Holzman I, Ober C, Peterson CM, Withiam MJ, Duckies A, Mueller-Heubach E, Polk BF, and the National Institute of Child Health and Human Development Diabetes in Early Pregnancy Study (1988): Lack of relation of increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis. N Engl J Med 318: 671-676.
-
(1988)
N Engl J Med
, vol.318
, pp. 671-676
-
-
Mills, J.L.1
Knopp, R.H.2
Simpson, J.L.3
Jovanovic-Peterson, L.4
Metzger, B.E.5
Holmes, L.B.6
Aarons, J.H.7
Brown, Z.8
Reed, G.F.9
Bieber, F.R.10
Van Allen, M.11
Holzman, I.12
Ober, C.13
Peterson, C.M.14
Withiam, M.J.15
Duckies, A.16
Mueller-Heubach, E.17
Polk, B.F.18
-
21
-
-
0014145834
-
Congenital cardiac disease associated with polysplenia. A developmental complex of bilateral 'left-sidedness'
-
Moller JH, Nakib A, Anderson RC, Edwards JE (1967): Congenital cardiac disease associated with polysplenia. A developmental complex of bilateral 'left-sidedness'. Circulation 36: 789-799.
-
(1967)
Circulation
, vol.36
, pp. 789-799
-
-
Moller, J.H.1
Nakib, A.2
Anderson, R.C.3
Edwards, J.E.4
-
23
-
-
0025728197
-
Visceroatrial heterotaxy syndrome in the NOD mouse with special reference to atrial situs
-
Morishima M, Ando M, Takao A (1991): Visceroatrial heterotaxy syndrome in the NOD mouse with special reference to atrial situs. Teratology 44: 91-100.
-
(1991)
Teratology
, vol.44
, pp. 91-100
-
-
Morishima, M.1
Ando, M.2
Takao, A.3
-
24
-
-
0020617135
-
Familial clustering of situs inversus totalis, and asplenia and polysplenia syndromes
-
Niikawa N, Kohsaka S, Mizumoto M, Hamada I, Kajii T (1983): Familial clustering of situs inversus totalis, and asplenia and polysplenia syndromes. Am J Med Genet 16: 43-47.
-
(1983)
Am J Med Genet
, vol.16
, pp. 43-47
-
-
Niikawa, N.1
Kohsaka, S.2
Mizumoto, M.3
Hamada, I.4
Kajii, T.5
-
25
-
-
0021826418
-
Editorial comment on the paper by de la Monte and Hutchins on familial polyasplenia
-
Opitz JM (1985): Editorial comment on the paper by de la Monte and Hutchins on familial polyasplenia. Am J Med Genet 21: 175-176.
-
(1985)
Am J Med Genet
, vol.21
, pp. 175-176
-
-
Opitz, J.M.1
-
27
-
-
0025967142
-
Polyasplenia, caudal deficiency, and agenesis of the corpus callosum
-
Rodriguez JI, Palacios J, Omeñaca F, Lorente M (1991): Polyasplenia, caudal deficiency, and agenesis of the corpus callosum. Am J Med Genet 38: 99-102.
-
(1991)
Am J Med Genet
, vol.38
, pp. 99-102
-
-
Rodriguez, J.I.1
Palacios, J.2
Omeñaca, F.3
Lorente, M.4
-
28
-
-
0016840564
-
Syndromes of asplenia and polysplenia. A review of cardiac and non-cardiac malformations in 60 cases with special reference to diagnosis and prognosis
-
Rose V, Izukawa T, Moës CAP (1975): Syndromes of asplenia and polysplenia. A review of cardiac and non-cardiac malformations in 60 cases with special reference to diagnosis and prognosis. Br Heart J 37: 840-852.
-
(1975)
Br Heart J
, vol.37
, pp. 840-852
-
-
Rose, V.1
Izukawa, T.2
Moës, C.A.P.3
-
30
-
-
0019781843
-
Asplenia and polysplenia syndromes with abnormalities of lateralisation in a sibship
-
Zlotogora J, Elian E (1981): Asplenia and polysplenia syndromes with abnormalities of lateralisation in a sibship. J Med Genet 18: 301-302.
-
(1981)
J Med Genet
, vol.18
, pp. 301-302
-
-
Zlotogora, J.1
Elian, E.2
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