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Article title matches
- Category:Craniosynostosis (47 bytes)
1: List of pages with the keyword Craniosynostosis
Page text matches
- 1uzp (9,706 bytes)
11: ...re syndrome characterized by a marfanoid habitus, craniosynostosis, characteristic dysmorphic facial features, skele... - 1uzk (8,243 bytes)
11: ...re syndrome characterized by a marfanoid habitus, craniosynostosis, characteristic dysmorphic facial features, skele... - 1uzj (8,164 bytes)
11: ...re syndrome characterized by a marfanoid habitus, craniosynostosis, characteristic dysmorphic facial features, skele... - 1emo (8,056 bytes)
11: ...re syndrome characterized by a marfanoid habitus, craniosynostosis, characteristic dysmorphic facial features, skele... - 1emn (8,070 bytes)
11: ...re syndrome characterized by a marfanoid habitus, craniosynostosis, characteristic dysmorphic facial features, skele... - 1oec (10,534 bytes)
11: ...cterized by poor mineralization of the calvarium, craniosynostosis, dysmorphic facial features, prenatal teeth, hypo... - 1agw (8,106 bytes)
11: ... osteoglophonic dwarfism. OGD is characterized by craniosynostosis, prominent supraorbital ridge, and depressed nasa... - 1apj (7,931 bytes)
10: ...re syndrome characterized by a marfanoid habitus, craniosynostosis, characteristic dysmorphic facial features, skele... - 1b1c (6,236 bytes)
11: ...talia. Antley-Bixler syndrome is characterized by craniosynostosis, radiohumeral synostosis present from the perinat... - 1djs (11,740 bytes)
10: ...cterized by poor mineralization of the calvarium, craniosynostosis, dysmorphic facial features, prenatal teeth, hypo... - 1fgi (8,116 bytes)
11: ... osteoglophonic dwarfism. OGD is characterized by craniosynostosis, prominent supraorbital ridge, and depressed nasa... - 1fgk (7,858 bytes)
10: ... osteoglophonic dwarfism. OGD is characterized by craniosynostosis, prominent supraorbital ridge, and depressed nasa... - 1ias (6,595 bytes)
11: ...aracterized by arterial tortuosity and aneurysms, craniosynostosis, hypertelorism, and bifid uvula or cleft palate. ... - 1ii4 (4,514 bytes)
23: Apert syndrome (AS) is characterized by craniosynostosis (premature fusion of cranial sutures) and severe ... - 1iil (4,514 bytes)
23: Apert syndrome (AS) is characterized by craniosynostosis (premature fusion of cranial sutures) and severe ... - 4igd (5,536 bytes)
11: ... highly arched eyebrows, cleft lip and/or palate, craniosynostosis, learning disability and genital, limb and vesico... - 1lmj (8,133 bytes)
11: ...re syndrome characterized by a marfanoid habitus, craniosynostosis, characteristic dysmorphic facial features, skele... - 1m9z (8,829 bytes)
10: ...aracterized by arterial tortuosity and aneurysms, craniosynostosis, hypertelorism, and bifid uvula or cleft palate. ... - 1mhd (4,485 bytes)
10: ...so manifest early-onset osteoarthritis. They lack craniosynostosis and mental retardation. Note=SMAD3 mutations have... - 1mjs (4,544 bytes)
10: ...so manifest early-onset osteoarthritis. They lack craniosynostosis and mental retardation. Note=SMAD3 mutations have...
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