(Q33675453)

28 July 2017

title

The profile of major congenital abnormalities in the United Arab Emirates (UAE) population (English)

1 reference

28 July 2017

0 references

al-Gazali LI

1

1 reference

28 July 2017

Dawodu AH

series ordinal

2

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28 July 2017

Sabarinathan K

series ordinal

3

1 reference

28 July 2017

Varghese M

series ordinal

4

1 reference

28 July 2017

language of work or name

English

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publication date

1 January 1995

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

32

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28 July 2017

issue

1

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28 July 2017

page(s)

7-13

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What proportion of congenital abnormalities can be prevented?

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Otospondylomegaepiphyseal dysplasia: report of three sibs and review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

A syndrome of osteogenesis imperfecta, optic atrophy, retinopathy and severe developmental delay in two sibs of consanguineous parents.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

A family study of craniosynostosis, with probable recognition of a distinct syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Consanguinity and complex cardiac anomalies with situs ambiguus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Congenital malformations in 10,000 consecutive births in a university hospital: need for genetic counseling and prenatal diagnosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Recurrence of holoprosencephaly in families with a positive history.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Congenital malformations. A report of a study of series of consecutive births in 24 centres

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Inborn errors of morphogenesis. A review of localized hereditary malformations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Association of parental consanguinity with decreased birth weight and increased rate of early death and congenital malformations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

The London Dysmorphology Database

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Inbreeding and the incidence of childhood genetic disorders in Karnataka, South India.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

The role of major gene in clubfoot

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Consanguinity related prenatal and postnatal mortality of the populations of seven Pakistani Punjab cities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Value of routine ultrasound scanning at 19 weeks: a four year study of 8849 deliveries

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Genetic counseling for patients with birth defects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Congenital abnormalities in newborns of consanguineous and nonconsanguineous parents

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

A family study of renal agenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Prenatal diagnosis of cystic kidney disease with ventriculomegaly: a report of six cases in two related sibships

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Radial ray defect and Robin sequence: a new syndrome?

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050171

The incidence of congenital malformations: a study of 5,964 pregnancies

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7897633

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Homozygosity mapping: familiarity breeds debility

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7897633

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7897633

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.32.1.7

1 reference

28 July 2017

1 reference

28 July 2017

1 reference