WA 0859 3970 0884 RAB Pembuatan Cafe Aesthetic Di Plupuh Sragen

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NF1
- Neurofibromatosis, Familial Spinal
- Fibrous Dysplasia Of Bone
- Cafe-Au-Lait Spots, Multiple
- Leopard Syndrome 1
- Legius Syndrome
- Watson Syndrome
- Moyamoya Disease 2
- Noonan Syndrome 6
- Neurofibromatosis
PTPN11
- Neurofibromatosis, Familial Spinal
- Leopard Syndrome 1
- Russell-Silver Syndrome, X-Linked
- Moyamoya Disease 2
- Noonan Syndrome 6
- Neurofibromatosis
- Seckel Syndrome 2
- Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia
RAF1
- Neurofibromatosis, Familial Spinal
- Leopard Syndrome 1
- Russell-Silver Syndrome, X-Linked
- Noonan Syndrome 6
- Seckel Syndrome 2
KRAS
- Neurofibromatosis, Familial Spinal
- Cafe-Au-Lait Spots, Multiple
- Leopard Syndrome 1
- Russell-Silver Syndrome, X-Linked
- Noonan Syndrome 6
- Mccune–albright Syndrome
- Marinesco–sjögren Syndrome
- Neurofibromatosis
- Seckel Syndrome 2
LZTR1
- Leopard Syndrome 1
- Russell-Silver Syndrome, X-Linked
- Neurofibromatosis, Type Iii, Mixed Central And Peripheral
- Noonan Syndrome 6
- Seckel Syndrome 2
BRAF
- Neurofibromatosis, Familial Spinal
- Cafe-Au-Lait Spots, Multiple
- Leopard Syndrome 1
- Legius Syndrome
- Noonan Syndrome 6
- Marinesco–sjögren Syndrome
- Neurofibromatosis
- Vascular Malformation
SOS1
- Neurofibromatosis, Familial Spinal
- Leopard Syndrome 1
- Russell-Silver Syndrome, X-Linked
- Noonan Syndrome 6
- Seckel Syndrome 2
PCNT
- Cafe-Au-Lait Spots, Multiple
- Moyamoya Disease 2
- Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii
- Seckel Syndrome 2
BRCA2
- Neurofibromatosis, Familial Spinal
- Cafe-Au-Lait Spots, Multiple
- Fanconi Anemia, Complementation Group P
- Fanconi Anemia, Complementation Group D1
- Bloom Syndrome
RIT1
- Leopard Syndrome 1
- Russell-Silver Syndrome, X-Linked
- Noonan Syndrome 6
- Seckel Syndrome 2
SPRED1
- Neurofibromatosis, Familial Spinal
- Legius Syndrome
- Watson Syndrome
- Noonan Syndrome 6
- Neurofibromatosis
MAP2K2
- Cafe-Au-Lait Spots, Multiple
- Leopard Syndrome 1
- Watson Syndrome
- Noonan Syndrome 6
MAP2K1
- Cafe-Au-Lait Spots, Multiple
- Leopard Syndrome 1
- Noonan Syndrome 6
ATR
- Fanconi Anemia, Complementation Group P
- Russell-Silver Syndrome, X-Linked
- Noonan Syndrome 6
- Seckel Syndrome 2
- Bloom Syndrome
CBL
- Moyamoya Disease 2
- Noonan Syndrome 6
- Bloom Syndrome
- Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia
NRAS
- Neurofibromatosis, Familial Spinal
- Leopard Syndrome 1
- Noonan Syndrome 6
BUB1B
- Cafe-Au-Lait Spots, Multiple
- Mosaic Variegated Aneuploidy Syndrome 2
SHOC2
- Leopard Syndrome 1
- Moyamoya Disease 2
- Noonan Syndrome 6
CENPJ
- Russell-Silver Syndrome, X-Linked
- Noonan Syndrome 6
- Seckel Syndrome 2
BLM
- Fanconi Anemia, Complementation Group P
- Bloom Syndrome