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/vufind/Search/Results?lookfor=%22Crenshaw%2C+Molly+M%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Crenshaw%2C+Molly+M%22&type=Person&sort=year
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PubPharm (14)
1
Congenital diaphragmatic hernia in siblings with PIGA-related congenital disorder of glycosylation
enthalten in:
American journal of medical genetics. Part A
| 2023
von
Crenshaw, M.
|
Thompson, L.
|
Piqué, D.
| +3
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2
Five siblings expand the spectrum of GPC6-related skeletal dysplasia
enthalten in:
American journal of medical genetics. Part A
| 2023
von
Crenshaw, M.
|
Meyers, M.
|
Brown, K.
| +7
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3
A novel remote monitoring device recapitulates sleep patterns in angelman syndrome
enthalten in:
Sleep medicine
| 2023
von
Crenshaw, M.
|
Thompson, T.
|
Carson, R.
| +4
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4
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype
enthalten in:
American journal of human genetics
| 2023
von
Hiatt, S.
|
Trajkova, S.
|
Sebastiano, M.
| +81
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5
An Atypical 15q11.2 Microdeletion Not Involving SNORD116 Resulting in Prader-Willi Syndrome
enthalten in:
Case reports in genetics
| 2023
von
Crenshaw, M.
|
Graw, S.
|
Slavov, D.
| +4
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6
Congenital diaphragmatic hernia in siblings with PIGA‐related congenital disorder of glycosylation
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2023
von
Crenshaw, M.
|
Thompson, L.
|
Piqué, D.
| +3
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7
Deleterious, protein-altering variants in the X-linked transcriptional coregulator
ZMYM3
in 22 individuals with a neurodevelopmental delay phenotype
enthalten in:
bioRxiv.org
| 2022
von
Hiatt, S.
|
Trajkova, S.
|
Sebastiano, M.
| +72
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8
Pheochromocytoma and paraganglioma : germline genetics and hereditary syndromes
enthalten in:
Endocrine oncology (Bristol, England)
| 2022
von
Turin, C.
|
Crenshaw, M.
|
Fishbein, L.
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9
Erratum : Orofacial overgrowth with peripheral nerve enlargement and perineuriomatous pseudo-onion bulb proliferations is part of the PIK3CA-related overgrowth spectrum
enthalten in:
HGG advances
| 2022
von
Koutlas, I.
|
Anbinder, A.
|
Alshagroud, R.
| +12
ErratumFor: HGG Adv. 2020 Aug 14;1(1):100009. - PMID 35047831
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10
Lessons Learned from a Quality Improvement Initiative : Adverse Childhood Experiences Screening in a Pediatric Clinic
enthalten in:
Pediatric quality & safety
| 2021
von
Crenshaw, M.
|
Owens, C.
|
Dow-Smith, C.
| +2
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1
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Zeitschriftentitel
2
American journal of medical genetics. Part A
2
HGG advances
1
American Journal of Medical Genetics Part C: Se...
1
American journal of human genetics
1
Case reports in genetics
1
Cold Spring Harbor molecular case studies
1
Endocrine oncology (Bristol, England)
1
Journal of pediatric orthopedics
1
Journal of the American Academy of Dermatology
1
Pediatric quality & safety
1
Sleep medicine
1
bioRxiv.org
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Thema
8
Journal Article
3
Case Reports
2
Research Support, Non-U.S. Gov't
2
overgrowth
1
2–3 toe syndactyly
1
570
1
AKT1
1
Angelman syndrome
1
Antigens, Neoplasm
1
Biology
1
CLUAP1 protein, human
1
Carrier Proteins
1
EC 1.14.11.-
1
EC 1.5.-
1
GPC6
1
GPC6 protein, human
1
Glypicans
1
Hedgehog Proteins
1
Histone Demethylases
1
Home monitoring
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Erscheinungszeitraum
11
2020-
3
2010-2019
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Englisch
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