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387 results on '"Pellissier, Jean-François"'

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51. Familial Cylindromatosis

52. Farabee Type Brachydactyly

53. Functional Vomiting

54. Flu Virus Infection

55. Focal Epilepsies of Adulthood, Idiopathic

56. Familial Hypocalciuric Hypercalcemia

57. Friedreich's Ataxia

58. Farber Lipogranulomatosis

59. Fructose Intolerance, Hereditary

60. Factor XI Deficiency

61. Familial Anterior Hypopituitarism

62. Familial Spastic Paraplegia

63. Frontal Temporal Lobar Degeneration

64. Familial Nonhemolytic Conjugated Hyperbilirubinemia with Normal Liver Histology

65. Familial Adenomatous Polyposis

66. Fitch Type

67. Familial Benign Hypercalcemia

68. Factor IX Deficiency

69. Familial Polymorphic Ventricular Tachycardia

70. Familial Pulmonary Arterial Hypertension

71. Familial Cortical Tremor with Epilepsy

72. Fibrofolliculomas with Trichodiscomas and Acrochordons

73. Factor V Leiden

74. Familial Ligand-defective Apolipoprotein B-100

75. Familial Combined Hyperlipidemia

76. Filiform Warts

77. Familial Startle Disease

78. Familial Cortical Myoclonic Tremor

79. Fumarylacetoacetate Hydrolase Deficiency

80. Focal Atrial Tachycardia

81. Female Pseudo-Turner Syndrome

82. Familial Benign Myoclonus Epilepsy with Adult Onset

83. Familial Renal Glucosuria

84. Functioning Sudoriparous Angiomatous Hamartoma

85. Focal Epithelial Hyperplasia

86. Functional Renal Failure

87. Fat Malabsorption

88. Familial Orthostatic Hypotensive Disorder, Streeten Type

89. Focal Proliferative Glomerulonephritis

90. Fragile X Syndrome E

91. Febrile Non-hemolytic Transfusion Reactions

92. Follicular Thyroid Cancer

93. Familial Essential Myoclonus and Epilepsy

94. Fetal Herpes Zoster Syndrome, Varicella Embryopathy

95. Functional Intestinal Obstruction

96. Familial Juvenile Hyperuricemic Nephropathy

97. Familial Hypoproteinemia with Lymphangiectatic Enteropathy

98. Flesh-Eating Syndrome

99. Factor VIII Deficiency

100. FHBL due to Apolipoprotein-B Deficiency

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