(Q35682457)

9 August 2017

title

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity (English)

1 reference

9 August 2017

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F Gurrieri

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M Muenke

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9 August 2017

C Bay

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9 August 2017

D H Yi

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9 August 2017

A L Collins

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9 August 2017

V P Johnson

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9 August 2017

R C Hennekam

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9 August 2017

G B Schaefer

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9 August 2017

L Weik

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9 August 2017

M S Lubinsky

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9 August 2017

language of work or name

English

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publication date

1 August 1994

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Proceedings of the National Academy of Sciences of the United States of America

9 August 2017

published in

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9 August 2017

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9 August 2017

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9 August 2017

page(s)

8102-8106

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Holoprosencephaly: a family showing dominant inheritance and variable expression

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Strategies for multilocus linkage analysis in humans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Microcephaly in familial holoprosencephaly

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Holoprosencephaly: a developmental field defect.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Cloning a selected fragment from a human DNA 'fingerprint': isolation of an extremely polymorphic minisatellite

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

A second-generation linkage map of the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Physical mapping of the holoprosencephaly critical region on chromosome 7q36.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Single central incisor in familial holoprosencephaly

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=44553

Familial holoprosencephaly associated with a translocation breakpoint at chromosomal position 7q36

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8058764

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.91.17.8102

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9 August 2017

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9 August 2017

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