551 results on '"Poot, Martin"'
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2. Evaluation of tag attachment techniques for plunge‐diving terns
3. The Legacy of George M. Martin: From Segmental Progeroid Syndromes to Antigeroid Syndromes.
4. Evaluating the effects of moonlight on the vertical flight profiles of three western palaearctic swifts
5. Gene-network analysis identifies susceptibility genes related to glycobiology in autism.
6. Social Foraging by Waterbirds in Shallow Coastal Lagoons in Ghana
7. Moonlight synchronous flights across three western palearctic swifts mirror size dependent prey preferences
8. Genes, Proteins, and Biological Pathways Preventing Chromothripsis
9. Shifting the Focus of Molecular Syndromology from Individual Diagnoses to Outcome Analyses
10. Range-wide patterns of population differentiation of Eurasian Black Terns (Chlidonias niger niger) related to use of discrete post-nuptial staging sites
11. First records for Sierra Leone of Eurasian Spoonbill Platalea Leucorodia, Northern Shoveler Anas clypeata and Terek Sandpiper Xenus cinereus
12. The Expanding Phenotypic Spectrum of NUP188 Variants Points Toward Multiple Biological Pathways
13. GPS-Tracking of Great Cormorants Phalacrocorax carbo sinensis Reveals Sex-Specific Differences in Foraging Behaviour
14. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects
15. A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12
16. The aeroecology of atmospheric convergence zones: the case of pallid swifts
17. Deep White Matter Cysts in a Patient with Aicardi-Goutières Syndrome and SAMHD1 Variants
18. Expanded Phenotypic Spectrum or Multiple Syndromes?
19. Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene
20. Balanced at First Sight, but in Reality out of Balance
21. Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands
22. Three de novo losses and one insertion within a pericentric inversion of chromosome 6 in a patient with complete absence of expressive speech and reduced pain perception
23. Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism
24. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
25. Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder
26. A Novel 6.14 Mb Duplication of Chromosome 8p21 in a Patient with Autism and Self Mutilation
27. Ruimtelijke analyse en trends benthos Voordelta
28. Analyse bruinvisgegevens en evaluatie monitoring Noordzee
29. Beschikbaarheid van vis voor visdieven rond Marker Wadden in juli 2020
30. Eindrapportage monitoring- en onderzoeksprogramma Natuurcompensatie Voordelta (PMR-NCV)
31. Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2→qter
32. Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathy
33. Precision Medicine: from Molecular Diagnoses to Treatment Opportunities in Medical Genetics
34. Prevalence and Phenotypic Impact of Robertsonian Translocations
35. Antisense may make sense of 1q44 deletions, seizures, and HNRNPU
36. No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder
37. Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†
38. Lessons for aging from Werner syndrome epigenetics
39. How Many Genes Does It Take?
40. Fanconi Anemia: A Syndrome of Anemia and Skeletal Malformations Progressing to a Gene Network Involved in Genomic Stability and Malignant Disease
41. Mutated NUP188 and Other Nucleoporins as Gateways to Developmental Syndromes
42. Chromothripsis and Duplications as Underappreciated Genomic Gremlins
43. Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletions†
44. A Duplication Including GATA4 Does Not Co-Segregate With Congenital Heart Defects
45. GPS-Tracking of Great Cormorants Phalacrocorax carbo sinensis Reveals Sex-Specific Differences in Foraging Behaviour.
46. An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants
47. Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
48. Mutations in Mediator Complex Genes CDK8, MED12, MED13, and MEDL13 Mediate Overlapping Developmental Syndromes
49. Waterbird Survey in the wetlands of South-Benin in 1996 & 1997
50. Visdieven in het IJsselmeergebied: broedplaatskeuze en broedsucces in een wetland met weinig dynamiek
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