-
1
-
-
0016164162
-
Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition
-
Pena S.D., and Shokeir M.H. Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition. J Pediatr 85 (1974) 373-375
-
(1974)
J Pediatr
, vol.85
, pp. 373-375
-
-
Pena, S.D.1
Shokeir, M.H.2
-
3
-
-
34249659397
-
Changes in fetal motility as a result of congenital disorders: an overview
-
de Vries J.I., and Fong B.F. Changes in fetal motility as a result of congenital disorders: an overview. Ultrasound Obstet Gynecol 29 (2007) 590-599
-
(2007)
Ultrasound Obstet Gynecol
, vol.29
, pp. 590-599
-
-
de Vries, J.I.1
Fong, B.F.2
-
4
-
-
0037110998
-
Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnoses
-
Witters I., Moerman P., and Fryns J.P. Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnoses. Am J Med Genet 113 (2002) 23-28
-
(2002)
Am J Med Genet
, vol.113
, pp. 23-28
-
-
Witters, I.1
Moerman, P.2
Fryns, J.P.3
-
6
-
-
25644442465
-
Molecular etiopathogenesis of limb girdle muscular and congenital muscular dystrophies: boundaries and contiguities
-
Guglieri M., Magri F., and Comi G.P. Molecular etiopathogenesis of limb girdle muscular and congenital muscular dystrophies: boundaries and contiguities. Clin Chim Acta 361 (2005) 54-79
-
(2005)
Clin Chim Acta
, vol.361
, pp. 54-79
-
-
Guglieri, M.1
Magri, F.2
Comi, G.P.3
-
7
-
-
0034194862
-
Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype
-
Brueton L.A., Huson S.M., Cox P.M., et al. Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype. Am J Med Genet 92 (2000) 1-6
-
(2000)
Am J Med Genet
, vol.92
, pp. 1-6
-
-
Brueton, L.A.1
Huson, S.M.2
Cox, P.M.3
-
8
-
-
0021961416
-
Effects of hypoxemic events on breathing, body movements, and heart rate variation: a study in growth-retarded human fetuses
-
Bekedam D.J., and Visser G.H. Effects of hypoxemic events on breathing, body movements, and heart rate variation: a study in growth-retarded human fetuses. Am J Obstet Gynecol 153 (1985) 52-56
-
(1985)
Am J Obstet Gynecol
, vol.153
, pp. 52-56
-
-
Bekedam, D.J.1
Visser, G.H.2
-
9
-
-
0026516218
-
The effect of intrauterine growth retardation on the quality of general movements in the human fetus
-
Sival D.A., Visser G.H., and Prechtl H.F. The effect of intrauterine growth retardation on the quality of general movements in the human fetus. Early Hum Dev 28 (1992) 119-132
-
(1992)
Early Hum Dev
, vol.28
, pp. 119-132
-
-
Sival, D.A.1
Visser, G.H.2
Prechtl, H.F.3
-
10
-
-
0022402419
-
Abnormal motor behaviour in anencephalic fetuses
-
Visser G.H., Laurini R.N., de Vries J.I., Bekedam D.J., and Prechtl H.F. Abnormal motor behaviour in anencephalic fetuses. Early Hum Dev 12 (1985) 173-182
-
(1985)
Early Hum Dev
, vol.12
, pp. 173-182
-
-
Visser, G.H.1
Laurini, R.N.2
de Vries, J.I.3
Bekedam, D.J.4
Prechtl, H.F.5
-
11
-
-
0020037066
-
Ultrasound movement patterns of fetuses with chromosome anomalies
-
Boué J., Vignal P., Aubrey J.P., Aubrey M.C., and Mc Aleese J.M. Ultrasound movement patterns of fetuses with chromosome anomalies. Prenat Diagn 1 (1982) 61-65
-
(1982)
Prenat Diagn
, vol.1
, pp. 61-65
-
-
Boué, J.1
Vignal, P.2
Aubrey, J.P.3
Aubrey, M.C.4
Mc Aleese, J.M.5
-
12
-
-
0029945288
-
Qualitative analysis of fetal movement patterns in the Neu-Laxova syndrome
-
Kainer F., Prechtl H.F., Dudenhausen J.W., and Unger M. Qualitative analysis of fetal movement patterns in the Neu-Laxova syndrome. Prenat Diagn 16 (1996) 667-669
-
(1996)
Prenat Diagn
, vol.16
, pp. 667-669
-
-
Kainer, F.1
Prechtl, H.F.2
Dudenhausen, J.W.3
Unger, M.4
-
14
-
-
0020456246
-
The emergence of fetal behaviour. I. Qualitative aspects
-
de Vries J.I., Visser G.H., and Prechtl H.F. The emergence of fetal behaviour. I. Qualitative aspects. Early Hum Dev 7 (1982) 301-322
-
(1982)
Early Hum Dev
, vol.7
, pp. 301-322
-
-
de Vries, J.I.1
Visser, G.H.2
Prechtl, H.F.3
-
16
-
-
0023871299
-
The emergence of fetal behaviour. III. Individual differences and consistencies
-
de Vries J.I., Visser G.H., and Prechtl H.F. The emergence of fetal behaviour. III. Individual differences and consistencies. Early Hum Dev 16 (1988) 85-103
-
(1988)
Early Hum Dev
, vol.16
, pp. 85-103
-
-
de Vries, J.I.1
Visser, G.H.2
Prechtl, H.F.3
-
17
-
-
0022345439
-
The emergence of fetal behaviour. II. Quantitative aspects
-
de Vries J.I., Visser G.H., and Prechtl H.F. The emergence of fetal behaviour. II. Quantitative aspects. Early Hum Dev 12 (1985) 99-120
-
(1985)
Early Hum Dev
, vol.12
, pp. 99-120
-
-
de Vries, J.I.1
Visser, G.H.2
Prechtl, H.F.3
-
18
-
-
0002253401
-
Analysis of Pena Shokeir phenotype
-
Hall J.G. Analysis of Pena Shokeir phenotype. Am J Med Genet 25 (1986) 99-117
-
(1986)
Am J Med Genet
, vol.25
, pp. 99-117
-
-
Hall, J.G.1
-
19
-
-
0021090597
-
Fetal akinesia deformation sequence: an animal model
-
Moessinger A.C. Fetal akinesia deformation sequence: an animal model. Pediatrics 72 (1983) 857-863
-
(1983)
Pediatrics
, vol.72
, pp. 857-863
-
-
Moessinger, A.C.1
-
20
-
-
34249663698
-
Fetal movements and postures: what do they mean for postnatal development?
-
Hopkins B., and Johnson S.P. (Eds), Praeger Publishers, Westport
-
de Vries J.I., and Hopkins B. Fetal movements and postures: what do they mean for postnatal development?. In: Hopkins B., and Johnson S.P. (Eds). Prenatal Development of Postnatal Functions (2005), Praeger Publishers, Westport 177-219
-
(2005)
Prenatal Development of Postnatal Functions
, pp. 177-219
-
-
de Vries, J.I.1
Hopkins, B.2
-
21
-
-
0025175242
-
Does reduction of amniotic fluid affect fetal movements?
-
Sival D.A., Visser G.H.A., and Prechtl H.F.R. Does reduction of amniotic fluid affect fetal movements?. Early Hum Dev 23 (1990) 233-246
-
(1990)
Early Hum Dev
, vol.23
, pp. 233-246
-
-
Sival, D.A.1
Visser, G.H.A.2
Prechtl, H.F.R.3
-
22
-
-
0028262454
-
Abnormal motor behaviour and developmental postmortem findings in a fetus with Fanconi anaemia
-
de Vries J.I., Laurini R.N., and Visser G.H. Abnormal motor behaviour and developmental postmortem findings in a fetus with Fanconi anaemia. Early Hum Dev 36 (1994) 137-142
-
(1994)
Early Hum Dev
, vol.36
, pp. 137-142
-
-
de Vries, J.I.1
Laurini, R.N.2
Visser, G.H.3
-
23
-
-
70649114610
-
-
Patrizia Ferrettis A.C.C.T.G.M. (Ed), John Wiley & Sons Ltd, Chichester, UK
-
Baraitser M. In: Patrizia Ferrettis A.C.C.T.G.M. (Ed). Uses of databases in dysmorphology in embryos, genes and birth defects (2008), John Wiley & Sons Ltd, Chichester, UK 19-26
-
(2008)
Uses of databases in dysmorphology in embryos, genes and birth defects
, pp. 19-26
-
-
Baraitser, M.1
-
24
-
-
0027501336
-
Fetal akinesia/hypokinesia sequence: prenatal diagnosis and intra-familial variability
-
Bacino C.A., Platt L.D., Garber A., et al. Fetal akinesia/hypokinesia sequence: prenatal diagnosis and intra-familial variability. Prenat Diagn 13 (1993) 1011-1019
-
(1993)
Prenat Diagn
, vol.13
, pp. 1011-1019
-
-
Bacino, C.A.1
Platt, L.D.2
Garber, A.3
-
25
-
-
0035085257
-
Pena-Shokeir phenotype with variable onset in three consecutive pregnancies
-
Paladini D., Tartaglione A., Agangi A., et al. Pena-Shokeir phenotype with variable onset in three consecutive pregnancies. Ultrasound Obstet Gynecol 17 (2001) 163-165
-
(2001)
Ultrasound Obstet Gynecol
, vol.17
, pp. 163-165
-
-
Paladini, D.1
Tartaglione, A.2
Agangi, A.3
-
26
-
-
0037082978
-
Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler type
-
Witters I., Moerman P., Devriendt K., et al. Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler type. Am J Med Genet 108 (2002) 41-44
-
(2002)
Am J Med Genet
, vol.108
, pp. 41-44
-
-
Witters, I.1
Moerman, P.2
Devriendt, K.3
-
27
-
-
0034831131
-
Fetal akinesia deformation sequence: behavioral development in a case of congenital myopathy
-
Mulder E.J., Nikkels P.G., and Visser G.H. Fetal akinesia deformation sequence: behavioral development in a case of congenital myopathy. Ultrasound Obstet Gynecol 18 (2001) 253-257
-
(2001)
Ultrasound Obstet Gynecol
, vol.18
, pp. 253-257
-
-
Mulder, E.J.1
Nikkels, P.G.2
Visser, G.H.3
-
28
-
-
38749153268
-
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients
-
Vogt J., Harrison B.J., Spearman H., et al. Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients. Am J Hum Genet 82 (2008) 222-227
-
(2008)
Am J Hum Genet
, vol.82
, pp. 222-227
-
-
Vogt, J.1
Harrison, B.J.2
Spearman, H.3
-
29
-
-
40749093330
-
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders
-
Michalk A., Stricker S., Becker J., et al. Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. Am J Hum Genet 82 (2008) 464-476
-
(2008)
Am J Hum Genet
, vol.82
, pp. 464-476
-
-
Michalk, A.1
Stricker, S.2
Becker, J.3
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