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L. Van Maldergem

Veröffentlichungen von L. Van Maldergem zu Van Maldergem, L.. ->
weitere Veröffentlichungen von L. Van Maldergem:
Atypical Features in Angelman Syndrome Due to Imprinting Defect or Uniparental Disomy of Chromosome 15 (2000)
Atypical Features in Angelman Syndrome Due to Imprinting Defect or Uniparental Disomy of Chromosome 15 (2000)
Atypical Features in Angelman Syndrome Due to Imprinting Defect or Uniparental Disomy of Chromosome 15 (2000)
Human liver pathology in peroxisomal diseases: A review including novel data (1993)
Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency (2000)
Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency (2000)
X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus (1991)
Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency (2000)
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings (2000)
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism (2003)
Veröffentlichungen zu Van Maldergem, L..
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1
Dan, B.. Atypical Features in Angelman Syndrome Due to Imprinting Defect or Uniparental Disomy of Chromosome 15
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 31, No. 02 (4. 2000), p. 109-110
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2000
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2
Dan, B.. Atypical Features in Angelman Syndrome Due to Imprinting Defect or Uniparental Disomy of Chromosome 15
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 31, No. 02 (4. 2000), p. 109-110
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2000
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3
Dan, B.., Boyd, S. G.., ... Atypical Features in Angelman Syndrome Due to Imprinting Defect or Uniparental Disomy of Chromosome 15
in: Neuropediatrics. - Stuttgart [u.a.] : Thieme, ISSN 1439-1899, Vol. 31, No. 02 (2000), p. 109-110
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2000
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4
Roels, F., Espeel, M., ... Human liver pathology in peroxisomal diseases: A review including novel data
in: Biochimie, in: Biochimie . - Amsterdam : Elsevier, ISSN 0300-9084, ZDB-ID 2011725-5 Vol. 75, No. 3-4 (1993), p. 281-292
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1993
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5
de Koning, T. J.. Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 31, No. 06 (12. 2000), p. 287-292
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2000
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6
de Koning, T. J.. Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 31, No. 06 (12. 2000), p. 287-292
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2000
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7
VanMaldergem, L., Espeel, M., ... X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus
in: Human genetics , ISSN 1432-1203, Vol. 87 (6. 1991), p. 661-664
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1991
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8
de Koning, T. J.., Jaeken, J.., ... Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency
in: Neuropediatrics. - Stuttgart [u.a.] : Thieme, ISSN 1439-1899, Vol. 31, No. 06 (2000), p. 287-292
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2000
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9
Van Maldergem, L., Tuerlinckx, D., ... Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings
in: European journal of pediatrics , ISSN 1432-1076, Vol. 159 (1/2. 2000), p. 108-112
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2000
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10
Jamain, Stéphane, Quach, Hélène, ... Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 34, No. 1 (2003), p. 27-29
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2003