Genetic heterogeneity of cebocephaly (Q33585937)

28 July 2017

title

Genetic heterogeneity of cebocephaly (English)

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28 July 2017

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Holmes LB

1

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28 July 2017

Driscoll S

series ordinal

2

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28 July 2017

Atkins L

series ordinal

3

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28 July 2017

language of work or name

English

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publication date

1 March 1974

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

11

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28 July 2017

issue

1

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28 July 2017

page(s)

35-40

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FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA

28 July 2017

cites work

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Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome

14 July 2018

1 reference

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Familial cebocephaly. Case description and survey of the anomaly.

14 July 2018

1 reference

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Males with a uterus and fallopian tubes, a rare disorder of sexual development

14 July 2018

1 reference

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Familial holoprosencephaly with endocrine dysgenesis.

14 July 2018

1 reference

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The "D" syndrome. Report of four trisomic and one D/D translocation case.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013086

A 46 CHROMOSOME CEBOCEPHALY, WITH REMARKS ON THE RELATION OF 13-15 TRISOMY TO HOLOPROSENCEPHALY (ARHINENCEPHALY).

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013086

Pathoarchitectonic studies of cerebral malformations. III. Arrhinencephalies (holotelencephalies).

31 October 2018

1 reference

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Consecutive hydrocephalics

31 October 2018

1 reference

12 December 2020

Short arm deletion of chromosome 18 in cebocephaly

1 reference

12 December 2020

On three cases of C trisomy

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12 December 2020

Objective measurement of interpupillary distance

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12 December 2020

A single nasal orifice and severe intrauterine growth retardation in a case of 46, XX, 18 r

1 reference

12 December 2020

[Trisomy 13-15 with cebocephaly]

1 reference

12 December 2020

CONGENITAL ANOMALIES IN THE NEWBORN INFANT, INCLUDING MINOR VARIATIONS. A STUDY OF 4,412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES AND BUCCAL SMEAR FOR SEX CHROMATIN

1 reference

12 December 2020

Identifiers

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28 July 2017

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