(Q34756479)

4 August 2017

title

Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition (English)

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4 August 2017

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Kjaer I

1

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4 August 2017

Niebuhr E

series ordinal

2

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4 August 2017

publication date

1 January 1999

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American Journal of Medical Genetics Part A

4 August 2017

published in

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4 August 2017

volume

82

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4 August 2017

issue

1

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4 August 2017

page(s)

6-14

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Pax genes and skeletal development

4 August 2017

cites work

1 reference

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Normal and abnormal growth of the mandible. A synthesis of longitudinal cephalometric implant studies over a period of 25 years.

21 January 2018

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A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#

Reversal of axonal pathways from rhombomere 3 correlates with extra Hox expression domains

21 January 2018

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Human prenatal craniofacial development related to brain development under normal and pathologic conditions

21 January 2018

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The development of the human brain and the closure of the rostral neuropore at stage 11.

21 January 2018

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The human brain at stages 21-23, with particular reference to the cerebral cortical plate and to the development of the cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#

The human larynx at the end of the embryonic period proper. 2. The laryngeal cavity and the innervation of its lining

21 January 2018

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21 January 2018

The cri du chat syndrome

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Cerebellar and brainstem hypoplasia in a child with a partial monosomy for the short arm of chromosome 5 and partial trisomy for the short arm of chromosome 10

21 January 2018

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Skeletal Changes in the «Cri du Chat» Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#

Measurements on hand radiographs from 32 cri-du-chat probands

21 January 2018

1 reference

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Pattern of malformations in the axial skeleton in human trisomy 18 fetuses

21 January 2018

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https://api.crossref.org/works/10.1002/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#

Pattern of malformations in the axial skeleton in human trisomy 13 fetuses

21 January 2018

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https://api.crossref.org/works/10.1002/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#

Cytologic observations in 35 individuals with a 5p- karyotype

21 January 2018

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Reexamination of the origin and early development of the human larynx

21 January 2018

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10.1002/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#

21 January 2018

Identifiers

DOI

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4 August 2017

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