(Q48247301)

9 February 2018

title

Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages (English)

1 reference

9 February 2018

1 reference

Al-Gazali LI

1

1 reference

9 February 2018

Sztriha L

2

1 reference

9 February 2018

Dawodu A

3

1 reference

9 February 2018

Bakir M

4

1 reference

9 February 2018

Varghese M

5

1 reference

9 February 2018

Varady E

6

1 reference

9 February 2018

Scorer J

7

1 reference

9 February 2018

Abdulrazzaq YM

8

1 reference

9 February 2018

Bener A

9

1 reference

9 February 2018

Padmanabhan R

10

1 reference

9 February 2018

publication date

1 February 1999

1 reference

9 February 2018

published in

Clinical Genetics

1 reference

9 February 2018

volume

55

1 reference

9 February 2018

issue

2

1 reference

9 February 2018

page(s)

95-102

1 reference

9 February 2018

Aspects of the incidence of central nervous system malformations in Cologne 1971-1980.

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Meckel syndrome and neural tube defects in Kuwait

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Agyria-pachygyria and agenesis of the corpus callosum: autosomal recessive inheritance with neonatal death

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Abnormal myelination in peroxisomal isolated dihydroxyacetonephosphate acyltransferase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Spina bifida--a vanishing nightmare?

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Anencephaly: disappearing in Kuwait?

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Time trends of spina bifida in Sweden 1947-81

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Epidemiology of infantile hydrocephalus in Sweden. I. Birth prevalence and general data

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

A survey of serious congenital morphological abnormalities in Abu Dhabi

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Easily identifiable congenital malformations in children: Survey of incidence and pattern in 32,332 live born neonates

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Anencephaly in Shiraz, Iran

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Etiologic heterogeneity of neural tube defects: clues from epidemiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Metabolic disorders of embryogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Autosomal recessive disorders among Arabs: an overview from Kuwait

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

High incidence of Meckel's syndrome in Gujarati Indians

21 January 2018

2 references

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

21 January 2018

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

Why do UK-born Pakistani babies have high perinatal and neonatal mortality rates?

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

Perinatal mortality in different ethnic groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

CNS malformations in the Kraków region. I. Birth prevalence and seasonal incidence during 1979-1981

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

Consanguineous marriages in the United Arab Emirates

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

Werdnig Hoffman's disease (spinal muscular atrophy type I): A clinical study of 25 Saudi nationals in Al-Khobar

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

Major congenital neurologic malformations. A 17-year survey.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

19-year incidence of neural tube defects in area under constant surveillance

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

Spina bifida and anencephaly in Scotland.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

Incidence of neural tube defects in Victoria, Australia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

Phenotypic heterogeneity in neural tube defects: a clue to causal heterogeneity

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

A five-year prospective study of the health of children in different ethnic groups, with particular reference to the effect of inbreeding.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550205.X

7 January 2021

10.1034/J.1399-0004.1999.550205.X

Identifiers

DOI

1 reference

9 February 2018

1 reference

9 February 2018