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51. Dynamics of a two-dimensional discrete-time SIS model

53. Severe Acute Pulmonary Toxicity Associated with Brentuximab in a Patient with Refractory Hodgkin’s Lymphoma

54. Performing a tarsorrhaphy

55. Funcionalidade global de idosos hospitalizados

56. Evaluation of frailty, functional capacity and quality of life of the elderly in geriatric outpatient clinic of a university hospital

58. Survey of family history taking and genetic testing in pediatric practice.

59. Beyond the Genetic Diagnosis: Providing Parents What They Want to Know.

61. Surveying the current landscape of clinical genetics residency training.

62. Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

63. Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder.

64. Genetic and genomic literacy in pediatric primary care.

65. Epigenetics and primary care.

67. Clinical utility of the X-chromosome array.

68. Improving newborn screening follow-up in pediatric practices: quality improvement innovation network.

69. Health supervision for children with fragile X syndrome.

70. How best to use CGH arrays in the clinical setting.

71. Fragile X syndrome detection in newborns-pilot study.

72. Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities.

74. Prenatal mucolipidosis type II (I-cell disease) can present as Pacman dysplasia.

76. Is Jaffe-Campanacci syndrome just a manifestation of neurofibromatosis type 1?

77. 22q13 deletion syndrome.

78. Shoulder response characteristics and injury due to lateral glenohumeral joint impacts.

79. Down syndrome clinic in a semi-rural setting.

80. Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.

81. Prenatal diagnosis of mosaic 4p- in a fetus with trisomy 21.

82. Brachmann-de Lange syndrome: diagnostic difficulties posed by the mild phenotype.

83. First impressions! The power of language in the health care setting.

84. Molecular genetic advances in fragile X syndrome.

85. Cytogenetic, biochemical, and molecular analyses of a 22q13 deletion.

86. DNA fingerprinting: the utilization of minisatellite probes to detect a somatic mutation in the proteus syndrome.

87. A "new" skeletal dysplasia in two unrelated boys.

88. Mental retardation in the Bannayan syndrome.

90. Deterioration of high-moisture corn.

93. Caffey's disease revisited. Further evidence for autosomal dominant inheritance with incomplete penetrance.

94. Fragile X syndrome in South Carolina.

97. Hyperplasia of the myenteric plexus. Its association with early infantile megacolon and neurofibromatosis.

98. Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina.

99. Microbiology of ensiled high-moisture corn.

100. Lactobacilli in ensiled high-moisture corn.

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