A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36. (Q34294770)

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20 October 2019

title

A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36 (English)

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20 October 2019

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8

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20 October 2019

Andrew J Copp

3

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20 October 2019

Rudi Balling

6

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20 October 2019

author name string

Lynch SA

1

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20 October 2019

Bond PM

2

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20 October 2019

Kirwan WO

4

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20 October 2019

Nour S

5

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20 October 2019

Mariman E

7

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20 October 2019

Strachan T

9

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20 October 2019

language of work or name

English

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publication date

1 September 1995

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20 October 2019

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20 October 2019

volume

11

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20 October 2019

issue

1

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20 October 2019

page(s)

93-95

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https://scigraph.springernature.com/pub.10.1038/ng0995-93

20 October 2019

exact match

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cites work

Patterning of mammalian somites by surface ectoderm and notochord: evidence for sclerotome induction by a hedgehog homolog

1 reference

Control of cell pattern in the neural tube: regulation of cell differentiation by dorsalin-1, a novel TGF beta family member

21 January 2018

1 reference

Function of retinoic acid receptor gamma in the mouse

21 January 2018

1 reference

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

21 January 2018

1 reference

The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q.

21 January 2018

1 reference

A new polydactyly/imperforate-anus/vertebral-anomalies syndrome?

21 January 2018

1 reference

Case reports of malformations associated with maternal diabetes: history and critique

21 January 2018

1 reference

Integrated human genome-wide maps constructed using the CEPH reference panel.

21 January 2018

1 reference

Sacral agenesis and caudal spinal cord malformations

21 January 2018

1 reference

7 January 2021

Triad of anorectal, sacral, and presacral anomalies

1 reference

7 January 2021

Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1

1 reference

7 January 2021

A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus.

1 reference

7 January 2021

Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele

1 reference

7 January 2021

Hereditary sacral agenesis with presacral mass and anorectal stenosis: the Currarino triad

1 reference

7 January 2021

Anorectal malformations with sacral bony abnormalities

1 reference

7 January 2021

Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers

1 reference

7 January 2021

The development of the human brain, the closure of the caudal neuropore, and the beginning of secondary neurulation at stage 12.

1 reference

7 January 2021

Does lumbosacral spina bifida arise by failure of neural folding or by defective canalisation?

1 reference

7 January 2021

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

1 reference

7 January 2021

A complex bilateral polysyndactyly disease locus maps to chromosome 7q36

1 reference

7 January 2021

Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter

1 reference

7 January 2021

An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly.

1 reference

7 January 2021

A computer program to make linkage analysis with LIPED and LINKAGE easier to perform and less prone to input errors

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0995-93

1 reference

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20 October 2019

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