(Q37156016)

18 August 2017

Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3. (English)

1 reference

18 August 2017

Abdul Noor

1

1 reference

18 August 2017

Christian Windpassinger

2

1 reference

18 August 2017

Irina Vitcu

3

1 reference

18 August 2017

Marija Orlic

4

1 reference

18 August 2017

Muhammad Arshad Rafiq

5

1 reference

18 August 2017

Mahwish Khalid

6

1 reference

18 August 2017

Mahmood Nasir Malik

7

1 reference

18 August 2017

Muhammad Ayub

8

1 reference

18 August 2017

Benjamin Alman

9

1 reference

18 August 2017

John B Vincent

10

1 reference

18 August 2017

language of work or name

English

0 references

publication date

2 April 2009

1 reference

American Journal of Human Genetics

18 August 2017

1 reference

18 August 2017

84

1 reference

18 August 2017

4

1 reference

18 August 2017

519-523

1 reference

Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Genome-wide association analysis identifies 20 loci that influence adult height

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Many sequence variants affecting diversity of adult human height

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Identification of ten loci associated with height highlights new biological pathways in human growth

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Osteopetrosis-like phenotype in latent TGF-beta binding protein 3 deficient mice

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Genetic approaches to stature, pubertal timing, and other complex traits

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Bone defects in latent TGF-beta binding protein (Ltbp)-3 null mice; a role for Ltbp in TGF-beta presentation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Mutation of PAX9 is associated with oligodontia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Radiographic assessment of hip and knee osteoarthritis. Recommendations: recommended guidelines

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Isolation of a novel latent transforming growth factor-beta binding protein gene (LTBP-3)

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

Missing maxillary lateral incisors: a genetic study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667979

The novel gene locus for agenesis of permanent teeth (He-Zhao deficiency) maps to chromosome 10q11.2.

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19344874

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19344874

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Anthropometric correlates of blood pressure in normotensive Pakistani subjects

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19344874

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2009.03.007

1 reference

18 August 2017

1 reference

18 August 2017

PubMed publication ID

19344874

1 reference