(Q41928844)

14 October 2017

title

Sutural cataract, retinitis pigmentosa, microcephaly and psychomotor retardation. A new autosomal recessive disorder? (English)

1 reference

14 October 2017

0 references

1 reference

Ippel PF

1

1 reference

14 October 2017

Wittebol-Post D

series ordinal

2

1 reference

14 October 2017

van Nesselrooij BP

series ordinal

3

1 reference

14 October 2017

Bijlsma JB

series ordinal

4

1 reference

14 October 2017

language of work or name

1 reference

1 September 1994

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14 October 2017

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14 October 2017

volume

15

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14 October 2017

issue

3-4

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14 October 2017

page(s)

121-127

1 reference

Cockayne syndrome: Review of 140 cases

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F13816819409057838

Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819409057838

Tapetoretinal degeneration in brothers with apparent Cohen syndrome: Nosology with Mirhosseini-Holmes-Walton syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819409057838

Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819409057838

Autosomal recessive microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy, and hypogenitalism. Micro syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819409057838

10.3109/13816819409057838

21 January 2018

Identifiers

DOI

1 reference

14 October 2017

1 reference