WA 0821 1305 0400 Repair XRF Laboratorium di Gorontalo Gorontalo [[Tiga Pillar]]

Deep Research Advanced Download Gene List

ERCC4
- Werner Syndrome
- Hypospadias
- Xeroderma Pigmentosum, Complementation Group F
- Cerebrooculofacioskeletal Syndrome 1
- Xfe Progeroid Syndrome
- Fanconi Anemia, Complementation Group O
ERCC6
- Xeroderma Pigmentosum, Complementation Group F
- Cerebrooculofacioskeletal Syndrome 1
- Cockayne Syndrome A
RECQL4
- Rapadilino Syndrome
- Bloom Syndrome
- Werner Syndrome
- Li–fraumeni Syndrome
- Baller–gerold Syndrome
- Fanconi Anemia, Complementation Group O
TP53
- Bloom Syndrome
- Werner Syndrome
- Abdominal Aortic Aneurysm
- Li–fraumeni Syndrome
- Xeroderma Pigmentosum, Complementation Group F
- Cerebrooculofacioskeletal Syndrome 1
- Colorectal Cancer, Hereditary Nonpolyposis, Type 4
- Cockayne Syndrome A
- Fanconi Anemia, Complementation Group O
WRN
- Bloom Syndrome
- Werner Syndrome
- Cerebrooculofacioskeletal Syndrome 1
- Fanconi Anemia, Complementation Group O
- Dna Repair-Deficiency Disorder
ERCC1
- Werner Syndrome
- Xeroderma Pigmentosum, Complementation Group F
- Cerebrooculofacioskeletal Syndrome 1
- Xfe Progeroid Syndrome
- Cockayne Syndrome A
- Fanconi Anemia, Complementation Group O
TFAP2A
- Branchiooculofacial Syndrome
- Abdominal Aortic Aneurysm
- Hypospadias
- Branchio-Oto-Renal Syndrome
BLM
- Bloom Syndrome
- Werner Syndrome
- Cerebrooculofacioskeletal Syndrome 1
- Colorectal Cancer, Hereditary Nonpolyposis, Type 4
- Fanconi Anemia, Complementation Group O
SIX1
- Branchiooculofacial Syndrome
- Branchio-Oto-Renal Syndrome
ERCC8
- Xeroderma Pigmentosum, Complementation Group F
- Cerebrooculofacioskeletal Syndrome 1
- Cockayne Syndrome A
EYA1
- Branchiooculofacial Syndrome
- Hypospadias
- Cerebrooculofacioskeletal Syndrome 1
- Branchio-Oto-Renal Syndrome
LIG4
- Bloom Syndrome
- Werner Syndrome
- Hypospadias
- Xeroderma Pigmentosum, Complementation Group F
- Lig4 Syndrome
CHEK2
- Bloom Syndrome
- Li–fraumeni Syndrome
- Colorectal Cancer, Hereditary Nonpolyposis, Type 4
- Fanconi Anemia, Complementation Group O
MSH2
- Bloom Syndrome
- Colorectal Cancer, Hereditary Nonpolyposis, Type 4
- Fanconi Anemia, Complementation Group O
MLH1
- Bloom Syndrome
- Werner Syndrome
- Li–fraumeni Syndrome
- Colorectal Cancer, Hereditary Nonpolyposis, Type 4
- Fanconi Anemia, Complementation Group O
TGFBR2
- Abdominal Aortic Aneurysm
- Hypospadias
- Uterine Rupture
- Colorectal Cancer, Hereditary Nonpolyposis, Type 4
- Aneurysm
MYH11
- Abdominal Aortic Aneurysm
- Aortic Aneurysm, Familial Thoracic 4
- Hypospadias
- Aneurysm
BRCA1
- Bloom Syndrome
- Werner Syndrome
- Li–fraumeni Syndrome
- Hypospadias
- Xeroderma Pigmentosum, Complementation Group F
- Colorectal Cancer, Hereditary Nonpolyposis, Type 4
- Fanconi Anemia, Complementation Group O
BRIP1
- Bloom Syndrome
- Werner Syndrome
- Hypospadias
- Xeroderma Pigmentosum, Complementation Group F
- Colorectal Cancer, Hereditary Nonpolyposis, Type 4
- Fanconi Anemia, Complementation Group O
SIX5
- Branchiooculofacial Syndrome
- Branchio-Oto-Renal Syndrome