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Article title matches
- Category:Noonan B (39 bytes)
1: List of pages with the keyword Noonan B - Category:Noonan syndrome (46 bytes)
1: List of pages with the keyword Noonan syndrome - Image:Noonan syndrome figure.jpg (0 bytes)
- Category:Noonan, B (40 bytes)
1: List of pages with the keyword Noonan, B - Category:Noonan, T (40 bytes)
1: List of pages with the keyword Noonan, T - Category:Noonan T (39 bytes)
1: List of pages with the keyword Noonan T
Page text matches
- 1uwh (7,452 bytes)
11: ...NS7) [MIM:[https://omim.org/entry/613706 613706]. Noonan syndrome is a disorder characterized by facial dy... - 1uwj (5,903 bytes)
11: ...NS7) [MIM:[https://omim.org/entry/613706 613706]. Noonan syndrome is a disorder characterized by facial dy... - 1far (7,762 bytes)
11: ...me is an autosomal dominant disorder allelic with Noonan syndrome. The acronym LEOPARD stands for lentigin... - 1faq (7,395 bytes)
11: ...me is an autosomal dominant disorder allelic with Noonan syndrome. The acronym LEOPARD stands for lentigin... - 4jai (5,083 bytes)
16: ...kew B, Josephson K, Jiang X, Shutes A, Shankar V, Noonan T, Garcia-Berrios G, Dong R, Dhanabal M, Tian H, ... - 4h34 (4,686 bytes)
11: ...lay, and a bleeding diathesis. Some patients with Noonan syndrome type 1 develop multiple giant cell lesio... - 8txe (6,866 bytes)
11: ...condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitempo... - 8txg (6,855 bytes)
11: ...condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitempo... - 8txh (6,882 bytes)
11: ...condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitempo... - 1awe (5,767 bytes)
10: ...11868160</ref> Defects in SOS1 are the cause of Noonan syndrome type 4 (NS4) [MIM:[https://omim.org/entr... - 1b47 (4,297 bytes)
11: ...drome characterized by a phenotype reminiscent of Noonan syndrome. Clinical features are highly variable, ... - 1dbh (3,799 bytes)
11: ...11868160</ref> Defects in SOS1 are the cause of Noonan syndrome type 4 (NS4) [MIM:[https://omim.org/entr... - 1fbv (4,514 bytes)
11: ...drome characterized by a phenotype reminiscent of Noonan syndrome. Clinical features are highly variable, ... - 4h1o (4,635 bytes)
11: ...lay, and a bleeding diathesis. Some patients with Noonan syndrome type 1 develop multiple giant cell lesio... - 1nf1 (7,228 bytes)
10: ...s characterized by manifestations of both NF1 and Noonan syndrome (NS). NS is a disorder characterized by ... - 1nvu (5,450 bytes)
11: ...11868160</ref> Defects in SOS1 are the cause of Noonan syndrome type 4 (NS4) [MIM:[https://omim.org/entr... - 1q9c (3,865 bytes)
11: ...11868160</ref> Defects in SOS1 are the cause of Noonan syndrome type 4 (NS4) [MIM:[https://omim.org/entr... - 1rfa (6,788 bytes)
10: ...me is an autosomal dominant disorder allelic with Noonan syndrome. The acronym LEOPARD stands for lentigin... - 1s9i (4,049 bytes)
11: ...condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitempo... - 1s9j (5,386 bytes)
11: ...condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitempo...
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