Category:Medical genetics task force articles
Appearance
Pages in category "Medical genetics task force articles"
The following 119 pages are in this category, out of approximately 1,234 total. This list may not reflect recent changes.
(previous page) (next page)T
- Category talk:Template-Class medical genetics articles
- Talk:Tetra-amelia
- Talk:Tetraamelia
- Talk:Tetrahydrobiopterin deficiency
- Talk:Tetrasomy 9p
- Talk:Tetrasomy X
- Talk:Thai symphalangism syndrome
- Talk:Thalassemia
- Talk:Thanatophoric dysplasia
- Talk:The Cancer Genome Atlas
- Talk:The Focus Foundation
- Talk:The Monarch Initiative
- Talk:Therapeutic gene modulation
- Talk:Thiamine responsive megaloblastic anemia syndrome
- Talk:Thickened earlobes-conductive deafness syndrome
- Talk:Thomsen disease
- Talk:Thoracic dysplasia-hydrocephalus syndrome
- Talk:Thyroid hormone resistance
- Talk:Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome
- Talk:Tic Talk
- Talk:Timothy syndrome
- Talk:Edward Tobinick
- Category talk:Top-importance medical genetics articles
- Talk:Tourette syndrome
- Category talk:Tourette syndrome organizations
- Talk:Tourette's syndrome
- Talk:Toxicogenomics
- Talk:Transduction (genetics)
- Talk:Transgenerational epigenetic inheritance
- Talk:Transmission disequilibrium test
- Talk:Treacher Collins syndrome
- Talk:Trimethylaminuria
- Talk:Trinucleotide repeat disorder
- Talk:Trisomy 8
- Talk:Trisomy 9
- Talk:Trisomy 16
- Talk:Trisomy 18
- Talk:Trisomy 21
- Talk:Trisomy 22
- Talk:Trisomy X
- Talk:Tuberous sclerosis
- Talk:Tumor suppressor gene
- Talk:Turner syndrome
- Talk:TwinsUK
- Talk:Tyrosinemia
U
V
- Talk:VACTERL association
- Talk:Van Buchem disease
- Talk:Van der Woude syndrome
- Talk:Vectors in gene therapy
- Talk:Victor Velculescu
- Talk:Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome
- Talk:Ventricular inversion
- Talk:Ventriculo-radial syndrome
- Talk:Very long-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Viljoen–Kallis–Voges syndrome
- Talk:Viral transduction
- Talk:Vitelliform macular dystrophy
- Talk:Von Willebrand disease
W
- Talk:Waardenburg anophthalmia syndrome
- Talk:Waardenburg syndrome
- Talk:WAGR syndrome
- Talk:Walker–Warburg syndrome
- Talk:Warkany syndrome 1
- Talk:Weismann-Netter–Stuhl syndrome
- Talk:Weissenbacher–Zweymüller syndrome
- Talk:Werner syndrome
- Talk:Weyer's ulnar ray/oligodactyly syndrome
- Talk:Whole genome sequencing
- Talk:Wiedemann–Rautenstrauch syndrome
- Wikipedia talk:WikiProject Medicine/Medical genetics task force
- Wikipedia talk:WikiProject Medicine/Medical genetics task force/Article advice
- Wikipedia talk:WikiProject Medicine/Medical genetics task force/Article rating
- Wikipedia talk:WikiProject Medicine/Medical genetics task force/Participants
- Talk:Wildervanck syndrome
- Talk:James T. Willerson
- Talk:Williams syndrome
- Talk:Wilson's disease
- Talk:Winchester syndrome
- Talk:Wiskott–Aldrich syndrome
- Talk:Witteveen–Kolk syndrome
- Talk:WNT4 deficiency
- Talk:Wolf–Hirschhorn syndrome
- Talk:Wolfram syndrome
- Talk:World Down Syndrome Day
- Talk:Worth syndrome
X
- Talk:X chromosome
- Talk:X-linked adrenal hypoplasia congenita
- Talk:X-linked AHC
- Talk:X-linked Charcot–Marie–Tooth disease
- Talk:X-linked dominant inheritance
- Talk:X-linked ichthyosis
- Talk:X-linked recessive inheritance
- Talk:Xeroderma pigmentosum
- Talk:Bing Xia
- Talk:XX gonadal dysgenesis
- Talk:XX male syndrome
- Talk:XXXXY syndrome
- Talk:XXXY syndrome
- Talk:XXXYY syndrome
- Talk:XY sex-determination system
- Talk:XYY syndrome
- Talk:XYYY syndrome