Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene. - Wikidata - awgldk - TriplyDB

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

http://www.wikidata.org/entity/Q33674055

about

Emery-Dreifuss syndrome Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28 Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative study.Frequent alterations of visual pigment genes in adrenoleukodystrophy Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.Gene deletions in X-linked muscular dystrophy.Color vision defects in adrenomyeloneuropathy.

P2860

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P2860

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

http://www.wikidata.org/entity/Q33674055

description

1986 nî lūn-bûn

@nan

1986 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1986 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

1986年の論文

@ja

1986年論文

@yue

1986年論文

@zh-hant

1986年論文

@zh-hk

1986年論文

@zh-mo

1986年論文

@zh-tw

1986年论文

@wuu

name

Emery-Dreifuss muscular dystro ...... nkage to the factor VIII gene.

@ast

Emery-Dreifuss muscular dystro ...... nkage to the factor VIII gene.

@en

type

label

Emery-Dreifuss muscular dystro ...... nkage to the factor VIII gene.

@ast

Emery-Dreifuss muscular dystro ...... nkage to the factor VIII gene.

@en

prefLabel

Emery-Dreifuss muscular dystro ...... nkage to the factor VIII gene.

@ast

Emery-Dreifuss muscular dystro ...... nkage to the factor VIII gene.

@en

P1433

Q33674055-774215CC-AA86-424A-B4CE-7A51FAE19513

P1476

Q33674055-298D6B5A-3C25-4112-AA92-86D21C7CB857

P2093

Q33674055-05FDC9D1-D0FA-4236-ABE9-BD2EE585BF6B

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Q33674055-FC9343A6-B76D-4B6B-AF3C-DC1C36AAE43D

P2860

Q33674055-0BA2C7CC-477C-4856-90DD-BFA1DA800B64

Q33674055-191CDE12-018F-4827-AFEE-8A7976427C1A

Q33674055-35DBF8C9-A6B5-465E-BD95-A6618A7A0ABE

Q33674055-5B029D97-2E90-4FAC-B4C2-08645365DE63

Q33674055-74828BEF-093E-4BCD-88E2-DE88C037DD9B

Q33674055-B34CBE89-4C58-4350-95BA-3BA7161B0325

Q33674055-C7EA460B-AC6A-45C0-A681-38D6615678C1

Q33674055-CDCBF703-27CB-4B3E-8CE9-F50BE9376BB8

Q33674055-FBD01EF9-AF92-4D8E-9A34-4D9D4AC76EAC

Q33674055-FE4B0668-CABB-43F8-AE46-F2A98AA94B00

P304

Q33674055-4101955C-CF24-44CD-94D2-775060EF7171

P31

Q33674055-E82B5B2D-E82A-46AC-B82B-386F1A0F3F3C

P407

Q33674055-23A9B402-1C7A-4E87-BA67-81F38FCDFBF5

P433

Q33674055-6A2AFA42-F2FD-40B2-8AD3-3587CF69614C

P478

Q33674055-AAB076DB-5764-4DC7-A4C1-83ED37175361

P577

Q33674055-0CA0B902-DA14-4F45-88A6-4EDB8B67A4F7

P698

Q33674055-673D47AF-11A1-4148-9880-8F0AB0E9AD5F

P932

Q33674055-C2E05994-0E84-4CB8-AE24-13BF5B2F1DA5

P1433

Journal of Medical Genetics

P1476

Emery-Dreifuss muscular dystro ...... nkage to the factor VIII gene.

@en

P2093

Affara NA

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

Borkowska J

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

Ferguson-Smith MA

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

Hausmanowa-Petrusewicz I

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

Jamieson DM

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

Johnston AW

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

Kelly K

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

Yates JR

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

Zaremba J

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

P2860

Unusual type of benign x-linked muscular dystrophy

X linked muscular dystrophy with contractures.

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.

The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

X-linked scapuloperoneal syndrome.

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes.

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene.

The genetic linkage map of the human X chromosome.

Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.

P304

587-590

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

P31

scholarly article

P407

P433

6

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

P478

23

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

P577

1986-12-01T00:00:00Z

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

P698

2879931

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

P932

1049841

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