Molecular Genetic | مركز البرج للتشخيص الوراثي

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Molecular Genetic Tests List

Molecular Genetic

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Laboratory Test Directory (1/336)

Molecular Genetic

عرض النتائج 1 - 100 من أصل 336

1. 11-Beta-Hydroxylase Deficiency Genetic Analysis

2. 21-Hydroxylase Genetic Analysis

3. Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency

4. Aarskog Syndrome

5. ACE (Angiotensin I-Converting Enzyme) Genotype Analysis

6. ADAMTS13 Whole gene analysis

7. Severe Congenital Neutropenia (Autosomal Recessive)

8. AGT M235T Genotyping

9. Familial Hyperlipidemia Genetic Analysis

10. Periodic Fever, Familial, Autosomal Dominant (TRAPS) Genetic Analysis

11. Lung Cancer

12. Achondroplasia Mutation Analysis

13. Acute Myeloid Leukemia Genetic Testing

14. Alpha Thalassemia Mutation Analysis

15. Alpha Thalassemia X-related Mental Retardation Syndrome

16. Alpha-1-Antitrypsin Genotyping

17. Alkaptonuria Sequence Analysis

18. Alport Syndrome Genetic Analysis

19. Alzheimer Disease Type [1 - 3 - 4] Genetic Analysis

20. Amyotrophic Lateral Sclerosis (ALS)

21. Androgen Receptor Gene Analysis

22. Angiotensin II Receptor, Type 1 (AGTR1)

23. Antithrombin 3 Deficiency

24. APC Mutation Analysis

25. APOE Genotyping - Alzheimer Disease Risk Factor

26. Arylsulfatase A Deficiency

27. Aromatase Deficiency Genetic Analysis

28. ARPKD Genetic Analysis

29. ARSACS Genetic Analysis

30. ARX Gene Mutation Analysis

31. AT1R CC Genotyping

32. Ataxia-Telangiectasia Genetic Analysis

33. Bardet - Biedl Syndrome Genetic Analysis

34. Barth Syndrome Genetic Analysis

35. Bartter Syndrome Type 1

36. Basal Cell Nevus Syndrome

37. Bernard-Soulier Syndrome

38. Beta Thalassemia Whole Gene Analysis

39. Biotinidase Deficiency Genetic Analysis

40. Birt-Hogg-Dube Syndrome Genetic Analysis

41. Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome

42. Borjeson-Forssman-Lehmann Syndrome Genetic Analysis

43. BRCA1 Mutation Analysis

44. BRCA2 Mutation Analysis

45. CADASIL Genetic Analysis

46. Canavan Syndrome Genetic Analysis

47. Responsiveness to Various FLT3 Inhibitors

48. Charcot-Marie-Tooth Neuropathy Type 1A Genetic Analysis

49. Charcot-Marie-Tooth Neuropathy Type 1B Genetic Analysis

50. Charcot-Marie-Tooth Neuropathy Type 1C Genetic Analysis

51. Charcot-Marie-Tooth Neuropathy Type 1D Genetic Analysis

52. Charcot-Marie-Tooth Neuropathy Type 1E Genetic Analysis

53. Charcot-Marie-Tooth Neuropathy Type 2

54. Charcot-Marie-Tooth Neuropathy Type 2E/1F Genetic Analysis

55. Charcot-Marie-Tooth, X-Linked Type 1

56. CMTX1 Whole Gene Analysis

57. Coffin-Lowry Syndrome

58. COL1A1/2 Related Osteogenesis Imperfecta

59. Connexin 32 Whole Gene Analysis

60. Cornelia de Lange Syndrome [1-2]

61. Crigler-Najjar Syndrome Type1, Type2 (CNS1, CNS2)

62. CRTAP Related Osteogenesis Imperfecta

63. CYP2C19 Genotiplemesi

64. CYP2C9 Genotyping

65. CYP2D6

66. Dandy Walker Syndrome

67. Danon Disease Genetic Analysis

68. Dent Disease 1 Genetic Testing

69. Dentatorubral-Pallidoluysian Atrophy (DRPLA) Genetic Analysis

70. Distal Renal Tubular Acidosis Autosomal Recessive; RTADR

71. Dystonia 1 ( DYT 1)

72. Dystrophic Epidermolysis Bullosa

73. DJ-1 Related Parkinson Disease

74. DMD/BMD Del/Dup Analysis

75. DMD/BMD Del/Dup Carrier Analysis

76. DMD/BMD Whole Gene Analysis

77. Dravet Syndrome

78. Ehlers Danlos Syndrome Type I

79. ENOS (NOS3 Polymorphism Analysis)

80. EPCR Genetic Analysis

81. Epidermolysis Bullosa Testing

82. Episodic Ataxia Type 2

83. Fabry Disease Whole Gene Analysis

84. Factor 10 Deficiency

85. Factor V Leiden Mutation Analysis

86. Factor X Deficiency

87. Fanconi-Bickel Syndrome

88. Farber Disease Genetic Analysis

89. Feingold Syndrome Genetic Analysis

90. Phenylketonuria (PKU) Genetic Analysis

91. FGFR2 Genetic Analysis

92. FMF 12 Mutations Analysis

93. FMF 40 Mutations Analysis

94. FMF Whole Gene Analysis

95. Focal Segmental Glomerulosclerosis Type [1 - 2 - 3]

96. Fragile X (CGG repeats)

97. Fraser Syndrome

98. Friedreich Ataxia Genetic Analysis

99. Frontometaphyseal Dysplasia

100. Frontotemporal Dementia With Parkinsonism-17 Genetic Analysis

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