FA | A | GA | B | C | Start | Stub | FL | List | Category | Disambig | FM | Project | Redirect | Template | NA | ??? |
3 | 0 | 22 | 147 | 284 | 430 | 135 | 0 | 11 | 80 | 1 | 1 | 4 | 104 | 1 | 1 | 1 |
Pages in category "C-Class medical genetics articles"
The following 84 pages are in this category, out of approximately 284 total. This list may not reflect recent changes.
(previous page) (next page)M
N
P
- Talk:Pancreaticobiliary maljunction
- Talk:PANO1
- Talk:Paramyotonia congenita
- Talk:Patau syndrome
- Talk:Pendred syndrome
- Talk:Penetrance
- Talk:Personalized onco-genomics
- Talk:Peutz–Jeghers syndrome
- Talk:Phenylalanine hydroxylase
- Talk:Philadelphia chromosome
- Talk:Photic sneeze reflex
- Talk:Ploidy
- Talk:Polydactyly
- Talk:Potocki–Lupski syndrome
- Talk:Prenatal testing
- Talk:Primary ciliary dyskinesia
- Talk:Primary familial brain calcification
- Talk:Progerin
- Talk:Pseudocholinesterase deficiency
- Talk:Pseudodeficiency alleles
- Talk:Pyruvate dehydrogenase deficiency
- Talk:Pyruvate kinase deficiency
R
S
- Talk:Sack–Barabas syndrome
- Talk:Saethre–Chotzen syndrome
- Talk:Saito–Kuba–Tsuruta syndrome
- Talk:Sandhoff disease
- Talk:Say–Meyer syndrome
- Talk:Selenium in biology
- Talk:Sex selection
- Talk:Sex-determining region Y protein
- Talk:Short-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Smith–Fineman–Myers syndrome
- Talk:Smith–Magenis syndrome
- Talk:SMPD1-associated Niemann–Pick disease
- Talk:Sonoda syndrome
- Talk:SPG15 (disease)
- Talk:Spinal and bulbar muscular atrophy
- Talk:Syndromic autism