Mulibrey
nanism ("MU scle- LI ver- BR ain- EY e
nanism"), also called Perheentupa syndrome and pericardial constriction with growth
Kaynak: Mulibrey nanismSee also : Mulibrey
nanism References Further reading: 2 citations. author Nagase T, Ishikawa K, Suyama M, et al. | title Prediction of the
Kaynak: TRIM37bone diseases, developmental : mulibrey
nanism C05.116.099.343.914 | Thanatophoric+Dysplasia thanatophoric dysplasia C05.116.099.370 |
Kaynak: List of MeSH codes (C05)This constellation is characteristic of Mulibrey
nanism , but has also been described in Russell-Silver syndrome and Turner syndrome
Kaynak: Triangular facedwarfism : mulibrey
nanism. C16.320.290 | Eye+Diseases,+Hereditary eye diseases, hereditary : C16.320.290.040 | Albinism albinism albinism,
Kaynak: List of MeSH codes (C16)title Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey
nanism | journal Nat. Genet. | volume 25 | issue 3 |
Kaynak: RAD51Cauthor Bangstad HJ | title Primordial birdheaded
nanism associated with progressive ataxia, early onset insulin resistant diabetes, goiter
Kaynak: Bangstad syndromewhere Tobby, the interviewer (a cynical and sarcastic person with
nanism, how use the jimmy five clothes, mickey ears and have a "Zacarias
Kaynak: Charges.com.brThree rare causes of dwarfism are included in the Finnish heritage: cartilage-hair hypoplasia , diastrophic dysplasia and Mulibrey
nanism .
Kaynak: Finnish heritage diseaseMul Muli–Mull : Mulibrey
nanism Müller–Barth–Menger syndrome Müllerian agenesis Müllerian aplasia Müllerian derivatives lymphangiectasia
Kaynak: List of diseases (M)Mulibrey
nanism. 253250 TRIM37 Mullerian aplasia and hyperandrogenism. 158330 WNT4 Multiple cutaneous and uterine leiomyomata. 150800
Kaynak: List of OMIM disorder codes