about
Development of the hearts of lizards and snakes and perspectives to cardiac evolutionMutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalA gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.Digital data and the 19th century teratology collection.Segmentation anomalies of vertebrae and ribs with other abnormalities of blastogenesis: syndromes or associations?Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.Absence of the spleen(s) in conjoined twins: a diagnostic clue of laterality defects? Radiological study of historical specimens.Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cellsPaleodysmorphology and paleoteratology: Diagnosing and interpreting congenital conditions of the skeleton in anthropological contexts.Smith-Lemli-Opitz syndrome diagnosed in a 130-year-old anatomical specimen.The anatomy in relation to injury of the lateral collateral ligaments of the ankle: a current concepts review.Postmortem imaging exposed: an aid in MR imaging of musculoskeletal structures.A review of the embryological development and associated developmental abnormalities of the sternum in the light of a rare palaeopathological case of sternal clefting.Pectus excavatum and carinatum.Detection of G1138A Mutation of the FGFR3 Gene in Tooth Material from a 180-Year-Old Museological Achondroplastic SkeletonAbnormal growth of the proximal femur due to apophyseal-epiphyseal coalescence resulting in coxa valga--a report of two cases in adolescents.Lost and found: The identification process of human bodies recovered from the North Sea.When the right (Drug) should be left: Prenatal drug exposure and heterotaxy syndrome.Towards a 3-dimensional atlas of the developing human embryo: the Amsterdam experience.An interactive three-dimensional digital atlas and quantitative database of human development.Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings.Reply to Hofmann et al.Development of a mRNA profiling multiplex for the inference of organ tissues.The hypertrabeculated (noncompacted) left ventricle is different from the ventricle of embryos and ectothermic vertebrates.Brachmann-de Lange syndrome "avant la lettre".On the many faces of Leber hereditary optic neuropathy.Trapezius aplasia: indications for a dual developmental origin of the trapezius muscle.Frederik Ruysch (1638-1731): Historical perspective and contemporary analysis of his teratological legacy.Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.Malformations of the axial skeleton in the museum Vrolik: II: craniosynostoses and suture-related conditionsThe development of the human notochordSinus venosus incorporation: contentious issues and operational criteria for developmental and evolutionary studiesColourimetric analysis of thermally altered human bone samples.[Severe complications following an adeno-tonsillectomy in a patient with Hunter's syndrome (MPS II)]The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chainNo evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriersRespiratory chain function in Leber's hereditary optic neuropathy: lack of correlation with clinical disease[Diseases caused by mitochondrial DNA mutations]
P50
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