Category:Stub-Class medical genetics articles
 | Administrators: Please do not delete this category as empty! This category may be empty occasionally or even most of the time. |
 FA |  A |  GA | B | C | Start | Stub | FL | List | Category | Disambig | FM | Project | Redirect | Template | NA | ??? | Total |
| 3 | 0 | 24 | 160 | 291 | 437 | 152 | 0 | 11 | 82 | 2 | 1 | 4 | 106 | 1 | 0 | 2 | 1,276 |
Pages in category "Stub-Class medical genetics articles"
The following 152 pages are in this category, out of 152 total. This list may not reflect recent changes.
A
- Talk:Absence deformity of leg-cataract syndrome
- Talk:Acorea, microphthalmia and cataract syndrome
- Talk:Advanced Therapy Medicinal Product
- Talk:AHDC1
- Talk:Al Gazali Sabrinathan Nair syndrome
- Talk:Alanyl-tRNA synthetase domain containing 1
- Talk:ALG1-CDG
- Talk:Allelic heterogeneity
- Talk:Amaurosis congenita, cone-rod type, with congenital hypertrichosis
- Talk:Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly
- Talk:Aortopulmonary septal defect
- Talk:Aphalangy-syndactyly-microcephaly syndrome
- Talk:Armed Forces DNA Identification Laboratory
- Talk:Asymmetric crying facies
B
C
- Talk:Camera–Marugo–Cohen syndrome
- Talk:Camptodactyly-taurinuria syndrome
- Talk:William Warrick Cardozo
- Talk:Cataract-ataxia-deafness syndrome
- Talk:Cation channel sperm-associated auxiliary subunit beta
- Talk:Cation channel sperm-associated auxiliary subunit delta
- Talk:Cation channel sperm-associated auxiliary subunit gamma
- Talk:Cation channel sperm-associated auxiliary subunit zeta
- Talk:Primarosa Chieri
- Talk:Chromosome 15q partial deletion
- Talk:Clinic for Special Children
- Talk:Coeliac UK
- Talk:Congenital disorder of glycosylation type IIc
- Talk:Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
- Talk:Cousin syndrome
- Talk:Crandall syndrome
- Talk:Craniorhiny
- Talk:Cryptorchidism-arachnodactyly-intellectual disability syndrome
D
- Talk:De Finetti diagram
- Talk:Deafness-vitiligo-achalasia syndrome
- Talk:Diagnostic Interview for Genetic Studies
- Talk:Dihydrofolate reductase deficiency
- Talk:Distinct anxiety
- Talk:Dolichonychia
- Talk:Double zinc ribbon and ankyrin repeat-containing protein 1
- Talk:Du Pan syndrome
- Talk:Dwarfism, low-birth-weight type with unresponsiveness to growth hormone
E
F
G
H
I
- Talk:Ichthyosis-intellectual disability-dwarfism-renal impairment
- Talk:Indian childhood cirrhosis
- Talk:Infantile spasms-broad thumbs syndrome
- Talk:Intellectual disability-spasticity-ectrodactyly syndrome
- Talk:Interleukin-1 receptor-associated kinase 1-binding protein 1
- Talk:Iris hypoplasia with glaucoma
L
M
- Talk:Marker chromosome
- Talk:Microcephaly deafness syndrome
- Talk:Mir-390 microRNA precursor family
- Talk:Mir-590 microRNA precursor family
- Talk:Mir-618 microRNA precursor family
- Talk:Mir-624 microRNA precursor family
- Talk:Mir-625 microRNA precursor family
- Talk:Mir-633 microRNA precursor family
- Talk:Mir-636 microRNA precursor family
- Talk:Mir-638 microRNA precursor family
- Talk:Mir-650 microRNA precursor family
- Talk:Mir-652 microRNA precursor family
- Talk:Mir-711 microRNA precursor family
- Talk:Mir-3180 microRNA precursor family
- Talk:Molecular risk assessment
- Talk:Monogenic obesity
- Talk:Moonrise (Wolfson book)
- Talk:D. Holmes Morton
- Talk:MPI-CDG
- Talk:Mutational meltdown
- Talk:Myelokathexis
N
P
S
- Talk:SACRAL syndrome
- Talk:Nadia Awni Sakati
- Talk:Say-Field-Coldwell syndrome
- Talk:Schimke syndrome
- Talk:Schmitt Gillenwater Kelly syndrome
- Talk:Seaver–Cassidy syndrome
- Talk:Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
- Talk:Sequence (medicine)
- Talk:Smith–Martin–Dodd syndrome
- Talk:SonicParanoid
- Talk:Spondylo-meta-epiphyseal dysplasia
- Talk:Spondylocamptodactyly
- Talk:St. Helena familial genu valgum