Finlay-Marks syndrome: Report of two siblings and review of literature (Q55982114)

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2 February 2020

title

Finlay-Marks syndrome: report of two siblings and review of literature (English)

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2 February 2020

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2

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2 February 2020

author name string

Prashant Naik

series ordinal

1

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2 February 2020

Deepti Chopra

series ordinal

3

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2 February 2020

Yogesh Gupta

series ordinal

4

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2 February 2020

language of work or name

English

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publication date

25 May 2012

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American Journal of Medical Genetics

2 February 2020

published in

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2 February 2020

volume

158A

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2 February 2020

issue

7

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2 February 2020

page(s)

1696-1701

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Hypotonia, developmental delay and features of scalp???ear???nipple syndrome in an inbred Arab family

2 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

PTPRF is disrupted in a patient with syndromic amastia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Ectodermal dysplasia, lipoatrophy, diabetes mellitus, and amastia: a second case of the AREDYLD syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Scalp-ear-nipple syndrome: additional manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Aplasia cutis congenita: a clinical review and proposal for classification

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Athelia: case report and review of the literature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Complete breast absence revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

A previously undescribed condition: tricho-odonto-onycho-dermal syndrome. A review of the tricho-odonto-onychial subgroup of ectodermal dysplasias

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

AREDYLD: a syndrome combining an acrorenal field defect, ectodermal dysplasia, lipoatrophic diabetes, and other manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Finlay-Marks Syndrome: Another sporadic case and additional manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Brief clinical report: new, autosomal dominant form of ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Probing the Gene eXpression Database for candidate genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

Ectodermal dysplasias: clinical and molecular review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35389

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.35389

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22639454%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

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