(Q56332783)

10

0 references

Maximilian Muenke

object named as

Maximilian Muenke

Fabienne Wavrant De Vrieze

11

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4

object named as

Fabienne Wavrant De Vrieze

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author name string

Mahim Jain

1

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Deeann Wallis

2

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Nathaniel H Robin

3

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John A Hardy

5

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Mohsen Ghadami

6

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Kristin Bosse

7

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Regina C Betz

American Journal of Medical Genetics

8

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language of work or name

English

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publication date

1 September 2008

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published in

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volume

146A

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issue

17

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page(s)

2308-11

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cites work

Transcriptome analysis of the murine forelimb and hindlimb autopod.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Prediction of mammalian microRNA targets

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Craniosynostosis and related limb anomalies

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Allele-sharing models: LOD scores and accurate linkage tests

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Parametric and nonparametric linkage analysis: a unified multipoint approach

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian family

7 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774842

HaploPainter: a tool for drawing pedigrees with complex haplotypes

30 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18680190