Datoteka:X-linked recessive.svg
Izgled
Veličina ovog PNG pregleda za ovu SVG datoteku: 395 × 600 piksela. Ostale rezolucije: 158 × 240 piksela | 316 × 480 piksela | 506 × 768 piksela | 674 × 1.024 piksela | 1.349 × 2.048 piksela | 600 × 911 piksela.
Izvorna datoteka (SVG datoteka, nominalno 600 × 911 piksela, veličina datoteke: 136 KB)
Historija datoteke
Kliknite na datum/vrijeme da vidite verziju datoteke iz tog vremena.
Datum/vrijeme | Smanjeni pregled | Dimenzije | Korisnik | Komentar | |
---|---|---|---|---|---|
trenutno | 01:52, 28 novembar 2014 | 600 × 911 (136 KB) | Kashmiri | Minor colour corrections | |
01:37, 28 novembar 2014 | 600 × 911 (129 KB) | Kashmiri | Minor corrections | ||
01:26, 28 novembar 2014 | 601 × 912 (129 KB) | Kashmiri | Description added as per original source image; layout improvements | ||
04:22, 14 novembar 2010 | 765 × 990 (79 KB) | Drsrisenthil | {{Information |Description=X-linked Recessive inheritance From http://ghr.nlm.nih.gov/ *Re-creation of entire image in svg format by drsrisenthil |Source=*File:XlinkRecessive.jpg |Date=2010-11-14 02:14 (UTC) |Author=*File:XlinkRecessive.jpg: |
Upotreba datoteke
Sljedećih 7 stranica koristi ovu datoteku:
Globalna upotreba datoteke
Sljedeći wikiji koriste ovu datoteku:
- Upotreba na ar.wikipedia.org
- Upotreba na az.wikipedia.org
- Upotreba na bg.wikipedia.org
- Upotreba na bn.wikipedia.org
- Upotreba na ca.wikipedia.org
- Upotreba na de.wikipedia.org
- Upotreba na de.wiktionary.org
- Upotreba na el.wikipedia.org
- Upotreba na en.wikipedia.org
- Duchenne muscular dystrophy
- Becker muscular dystrophy
- Lesch–Nyhan syndrome
- Wiskott–Aldrich syndrome
- X-linked ichthyosis
- Norrie disease
- X-linked agammaglobulinemia
- Dyskeratosis congenita
- Ayazi syndrome
- IPEX syndrome
- Simpson–Golabi–Behmel syndrome
- Oculocerebrorenal syndrome
- Hunter syndrome
- McLeod syndrome
- SCARF syndrome
- Hypohidrotic ectodermal dysplasia
- Hyper-IgM syndrome type 1
- Aarskog–Scott syndrome
- Properdin deficiency
- Dent's disease
- Allan–Herndon–Dudley syndrome
- Ocular albinism type 1
- Ichthyosis follicularis with alopecia and photophobia syndrome
- Immunodeficiency with hyperimmunoglobulin M
- X-linked spinal muscular atrophy type 2
- Lisch epithelial corneal dystrophy
- Albinism–deafness syndrome
- X-linked myotubular myopathy
- Smith–Fineman–Myers syndrome
- Mohr–Tranebjærg syndrome
- Morgagni–Stewart–Morel syndrome
- Renpenning's syndrome
- Nasodigitoacoustic syndrome
- Myopathy, X-linked, with excessive autophagy
- XMEN disease
- User:Ozzie10aaaa/med edit/lab
- X-linked dystonia parkinsonism
- Hoyeraal–Hreidarsson syndrome
- X-linked thrombocytopenia
- L1 syndrome
Pogledajte globalne upotrebe ove datoteke.