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/vufind/Search/Results?lookfor=%22Hing%2C+Anne+V%22&type=Person&sort=year
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PubPharm (58)
1
Isolated frontosphenoidal craniosynostosis : An argument for genetic testing
enthalten in:
American journal of medical genetics. Part A
| 2023
von
Hodapp, M.
|
Hing, A.
|
Gallagher, E.
| +2
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2
Damaging variants in FOXI3 cause microtia and craniofacial microsomia
enthalten in:
Genetics in medicine : official journal of the American College of Medical Genetics
| 2023
von
Quiat, D.
|
Timberlake, A.
|
Curran, J.
| +23
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3
Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence
enthalten in:
American journal of medical genetics. Part A
| 2021
von
Wenger, T.
|
Perkins, J.
|
Parish-Morris, J.
| +14
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4
Targeted long-read sequencing identifies missing disease-causing variation
enthalten in:
American journal of human genetics
| 2021
von
Miller, D.
|
Sulovari, A.
|
Wang, T.
| +48
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5
Haploinsufficiency of SF3B2 causes craniofacial microsomia
enthalten in:
Nature communications
| 2021
von
Timberlake, A.
|
Griffin, C.
|
Heike, C.
| +27
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6
Reply : MN1 gene loss-of-function mutation causes cleft palate in a pedigree
enthalten in:
Brain : a journal of neurology
| 2021
von
Vegas, N.
|
Low, K.
|
Mak, C.
| +6
CommentOn: Brain. 2019 Jan 1;143(1):55-68. - PMID 31834374
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7
Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2021
von
Wenger, T.
|
Perkins, J.
|
Parish‐Morris, J.
| +14
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8
Targeted long-read sequencing resolves complex structural variants and identifies missing disease-causing variants
enthalten in:
bioRxiv.org
| 2020
von
Miller, D.
|
Sulovari, A.
|
Wang, T.
| +34
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9
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate
enthalten in:
American journal of human genetics
| 2018
von
Cox, L.
|
Cox, T.
|
Moreno Uribe, L.
| +30
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10
Novel findings of left ventricular non-compaction cardiomyopathy, microform cleft lip and poor vision in patient with SMC1A-associated Cornelia de Lange syndrome
enthalten in:
American journal of medical genetics. Part A
| 2017
von
Wenger, T.
|
Chow, P.
|
Randle, S.
| +8
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Zeitschriftentitel
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American journal of medical genetics. Part A
9
American journal of human genetics
5
American journal of medical genetics / C
3
Birth defects research. Part A, Clinical and mo...
3
The Cleft palate-craniofacial journal : officia...
2
American journal of medical genetics
2
Genetics in medicine : official journal of the ...
2
Molecular cytogenetics
2
Nature genetics
2
Pediatrics
2
Plastic and reconstructive surgery
2
Teratology
2
The Journal of craniofacial surgery
2
The cleft palate-craniofacial journal
1
AJR. American journal of roentgenology
1
American Journal of Medical Genetics Part C: Se...
1
Brain : a journal of neurology
1
Nature communications
1
Orthodontics & craniofacial research
1
Plastic and reconstructive surgery. Global open
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Thema
34
Journal Article
19
Research Support, N.I.H., Extramural
19
Research Support, Non-U.S. Gov't
9
Review
7
Case Reports
3
Core Binding Factor Alpha 1 Subunit
3
DNA-Binding Proteins
3
RUNX2 protein, human
3
cleft palate
2
Adaptor Proteins, Signal Transducing
2
Multicenter Study
2
Nuclear Proteins
2
TWIST1 protein, human
2
Tumor Suppressor Proteins
2
Twist-Related Protein 1
1
22q11del
1
AMER1 protein, human
1
CHD7 protein, human
1
Cadherins
1
Catenins
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Erscheinungszeitraum
55
2000-
3
1900-1999
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Englisch
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