(Q24323098)

roof of mouth development

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

Ophir Klein

18

0 references

Geert Mortier

Geert R Mortier

23

0 references

Derek Wong

Derek A Wong

34

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Arlene Drack

Arlene V Drack

13

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Usha Kini

17

Usha Kini

0 references

Wendy S Meschino

22

Wendy S Meschino

0 references

Rhonda E Schnur

29

Rhonda E Schnur

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author name string

Jeff M Milunsky

1

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Tom M Maher

2

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Geping Zhao

3

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Zhenyuan Wang

4

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John B Mulliken

5

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David Chitayat

6

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Michele Clemens

7

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Heather J Stalker

8

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Mislen Bauer

9

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Michele Burch

10

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Sébastien Chénier

11

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Michael L Cunningham

12

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Sandra Janssens

14

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Audrey Karlea

15

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Regan Klatt

16

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Augusta M Lachmeijer

19

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Andre Megarbane

20

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Nancy J Mendelsohn

21

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Sandhya Parkash

24

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C Renai Ray

25

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Angharad Roberts

26

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Amy Roberts

27

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Willie Reardon

28

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Rosemarie Smith

30

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Miranda Splitt

31

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Kamer Tezcan

32

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Margo L Whiteford

33

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Roberto Zori

35

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Angela E Lin

American Journal of Medical Genetics Part A

36

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language of work or name

English

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publication date

January 2011

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published in

1 reference

Branchio-oculo-facial syndrome with cleft lip and bilateral dermal thymus.

PubMed

volume

155A

0 references

issue

1

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page(s)

22-32

0 references

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Temporal bone anomalies in the branchio-oto-renal syndrome: detailed computed tomographic and magnetic resonance imaging findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Transcription factor AP-2 and monoaminergic functions in the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Recurrence of orbital cysts in the branchio-oculo-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

New autosomal dominant branchio-oculo-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Redundant activities of Tfap2a and Tfap2c are required for neural crest induction and development of other non-neural ectoderm derivatives in zebrafish embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Further delineation of the branchio-oculo-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Lesser forms of cleft lip associated with the branchio-oculo-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

TFAP2A mutations result in branchio-oculo-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Confirmation of TFAP2A gene involvement in branchio-oculo-facial syndrome (BOFS) and report of temporal bone anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Histology and synchrotron radiation-based microtomography of the inner ear in a molecularly confirmed case of CHARGE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Additional clinical and molecular analyses ofTFAP2Ain patients with the branchio-oculo-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Additional clinical and molecular analyses of TFAP2A in patients with the Branchio-Oculo-Facial syndrome: Previously reported patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

7 January 2021

A complexTFAP2Aallele is associated with branchio-oculo-facial syndrome and inner ear malformation in a deaf child

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

7 January 2021

Branchio-oculo-facial syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

7 January 2021

Branchio-oculo-facial syndrome associated with a white forelock

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33783

7 January 2021

Identifiers

DOI

10.1002/AJMG.A.33783

1 reference

Consolidated OpenCitations Corpus – April 2017

1663126

1663126

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference