Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy. - Wikidata - wikimedia - TriplyDB

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

http://www.wikidata.org/entity/Q33682728

about

Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophy Mutations in IMPG1 cause vitelliform macular dystrophies.Still no evidence for heterogeneity in Best's vitelliform macular dystrophy.

P2860

Q33680132-C4B4C75A-D95B-4893-81EE-DC84B40E9BA7 Q37162558-52B87C75-0516-4590-B22F-5EE75C655922 Q41930072-59CEE96D-1321-4A84-A508-F77EE9033949

P2860

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

http://www.wikidata.org/entity/Q33682728

description

1995 nî lūn-bûn

@nan

1995 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1995 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

1995年の論文

@ja

1995年論文

@yue

1995年論文

@zh-hant

1995年論文

@zh-hk

1995年論文

@zh-mo

1995年論文

@zh-tw

1995年论文

@wuu

name

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

@ast

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

@en

type

label

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

@ast

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

@en

prefLabel

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

@ast

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

@en

P1433

Q33682728-B180D918-9DE7-4C66-825D-B5CBFBFF2544

P1476

Q33682728-1570C3BE-3B71-4066-B912-F3C908DD3B56

P2093

Q33682728-0CB27BFB-01A6-45D2-8ED7-633232B39D56

Q33682728-117D0FC8-FF17-4850-BB35-320CBD8E6693

Q33682728-364098AF-71DD-4534-AE67-367E0D5CD430

Q33682728-38C4CE2A-6C14-4732-B434-4D4B89E3A052

Q33682728-8048EE2F-5D98-476C-A73B-3D04F7A298D5

Q33682728-C0A08D60-FC62-4119-BB19-9C7A03C5A46A

Q33682728-D3480569-A526-4CF1-B3CB-4B7B79BAE2B1

Q33682728-FCAADCB4-D238-4ED9-8511-260135F15EDF

P2860

Q33682728-01396AE3-7E90-45DA-8B4F-0DBB2B0C3DA8

Q33682728-0D26DC9C-A5D7-4A08-B63D-4B54E01E53FA

Q33682728-11C1FC0B-92E7-41AB-B720-A9E9F1B917DA

Q33682728-2916588B-B9CB-4984-9D1C-4191A7058AD0

Q33682728-536FA057-9E95-4BA9-B437-29218C245501

Q33682728-55565575-AF31-4309-8152-E16138DFC10D

Q33682728-77B7D484-D1E9-4F18-A9C6-5295B7489AC5

Q33682728-780079AF-D569-42A9-873A-62C632CA4E01

Q33682728-7B0656C0-2960-43FC-A506-A527A4067759

Q33682728-81132719-574E-4A94-8B83-932DA9EEA444

P304

Q33682728-91F59B30-54E7-4C1C-9DF3-FB93A1CF1135

P31

Q33682728-0D81FF98-F511-4F1D-BB52-594356F5DDA2

P356

Q33682728-324EEADB-EF0E-4F36-BD87-367058E82DD2

P407

Q33682728-4EEEA85E-3CBF-4FE5-B205-3205981320E6

P433

Q33682728-C17D5D43-AF44-453F-AAF0-7A64A431551F

P478

Q33682728-B38AB87F-0DD9-4198-B3A3-D3B6ABED5D9F

P50

Q33682728-13B4DA68-15F5-44CA-998B-F6FB69CF8731

Q33682728-E8AA6087-0EA2-426C-9207-28B3B7C2B5B9

P577

Q33682728-C446573A-C31B-42C1-8B32-5CC18C4F94F2

P5875

Q33682728-A32EED1A-AB7A-4A81-9D63-9345EC4FB284

P698

Q33682728-AF389317-6ABF-4965-8024-AC154AADF633

P932

Q33682728-B3F5B55E-AF08-4DFC-92BD-86CE407B0CCE

P356

P1433

Journal of Medical Genetics

P1476

Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

@en

P2093

A M Hally

http://www.w3.org/2001/XMLSchema#string

G J Farrar

http://www.w3.org/2001/XMLSchema#string

G Rudolph

http://www.w3.org/2001/XMLSchema#string

J Scorer

http://www.w3.org/2001/XMLSchema#string

L Mynett-Johnson

http://www.w3.org/2001/XMLSchema#string

M M Humphries

http://www.w3.org/2001/XMLSchema#string

P F Kenna

http://www.w3.org/2001/XMLSchema#string

R Kumar-Singh

http://www.w3.org/2001/XMLSchema#string

P2860

A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa

Strategies for multilocus linkage analysis in humans

The gene for Best's macular dystrophy is located at 11q13 in a Swedish family

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population

A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

P304

855-858

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1136/JMG.32.11.855

http://www.w3.org/2001/XMLSchema#string

P407

P433

11

http://www.w3.org/2001/XMLSchema#string

P478

32

http://www.w3.org/2001/XMLSchema#string

P50

Thomas Meitinger

P577

1995-11-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

14608877

http://www.w3.org/2001/XMLSchema#string

P698

8592326

http://www.w3.org/2001/XMLSchema#string

P932

1051734

http://www.w3.org/2001/XMLSchema#string