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4. A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

6. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech

17. Spectrum of NSD1 mutations in Sotos and Weaver syndromes

19. Complete DNA sequence of yeast chromosome XI

25. Deletion of the SIM1 gene (6q 16.2) in a patient with a Prader-Willi-like phenotype. (Letter to JMG)

26. Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders

32. The Yeast Genome Directory

37. Molecular analysis of Pericentrin gene (PCNT) in a series of 24 Seckel/ MOPD II families

38. Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

39. Technical comment: Response to comment on 'Tequila, a neurotrypsin ortholog, regulates long-term memory formation in Drosophila'

40. Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth

41. A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination

42. A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination

43. A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

44. A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features.

45. A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

47. Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families

50. Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1

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