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51. Individual common variants exert weak effects on the risk for autism spectrum disorderspi

52. A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features

53. Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype

54. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

55. SHANK1 Deletions in Males with Autism Spectrum Disorder

56. Haploinsufficiency of SF3B4, a Component of the Pre-mRNA Spliceosomal Complex, Causes Nager Syndrome

58. Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

59. Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder

60. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

61. Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder

62. A genome-wide scan for common alleles affecting risk for autism

63. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

64. Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival

65. Prophylactic total gastrectomy (PTG) for hereditary diffuse gastric cancer (HDGC): the Newfoundland experience with 23 patients

66. Spina bifida before and after folic acid fortification in Canada

67. Structural variation of chromosomes in autism spectrum disorder

68. Impact of folic acid food fortification on the birth prevalence of lipomyelomeningocele in Canada

69. Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer

70. ISDN2014_0253: High resolution genomic analyses of a clinically defined autism spectrum disorder cohort

71. Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

72. Male-to-female sex reversal associated with an approximately 250 kb deletion upstream of NR0B1 (DAX1)

73. An inversion inv(4)(p12–p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster

74. Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year prospective, population-based, cohort study

75. Human chromosome 7: DNA sequence and biology

76. Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder

77. Breast Cancer Events Associated with Germline Mutations of the CDH1 Gene (Hereditary Diffuse Gastric Cancer)

78. Erratum: Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

79. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

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