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Natalie Blagowidow
Observed name:
N. Blagowidow
Institution:
Greater Baltimore Medical Center
Observed institutions:
Northwestern University,
Greater Baltimore Medical Center,
Crozer-Keystone Health System,
Cornelia de Lange Syndrome Foundation,
Arcadia University,
University of Pennsylvania
show all 6
ORCID:
0000-0002-6655-2444
Observed ORCID:
0000-0002-6655-2444
OpenAlex ID:
A5069742720
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement
2018
·
Antonie D. Kline
, Joanna F. Moss
, et al.
·
Nature Reviews Genetics
·
398
PDF
Natural history of aging in Cornelia de Lange syndrome
2007
·
Antonie D. Kline
, Marco Grados
, et al.
·
American Journal of Medical Genetics Part C Seminars in Medical Genetics
·
179
PDF
XY gonadal dysgenesis: Genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis
1981
·
JoeLeigh Simpson
, Natalie Blagowidow
, et al.
·
Human Genetics
·
89
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions
2023
·
Natalie Blagowidow
, Beata Nowakowska
, et al.
·
Genes
·
38
PDF
Ullrich‐Turner syndrome in an XY female fetus with deletion of the sex‐determining portion of the Y chromosome
1989
·
Natalie Blagowidow
, David C. Page
, et al.
·
American Journal of Medical Genetics
·
27
Cornelia de Lange syndrome: Extending the physical and psychological phenotype
2010
·
Chris Oliver
, Maria Francesca Bedeschi
, et al.
·
American Journal of Medical Genetics Part A
·
26
Submicroscopic deletion in cousins with Prader‐Willi syndrome causes a grandmatrilineal inheritance pattern: Effects of imprinting
2000
·
Jeffrey E. Ming
, Natalie Blagowidow
, et al.
·
American Journal of Medical Genetics
·
24
Management of childbearing with hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders: A scoping review and expert co-creation of evidence-based clinical guidelines
2024
·
Sally Pezaro
, Isabelle Brock
, et al.
·
PLoS ONE
·
12
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation
2024
·
Elizabeth Goldmuntz
, Anne S. Bassett
, et al.
·
Prenatal Diagnosis
·
11
PDF
Obstetrics and gynecology in Ehlers‐Danlos syndrome: A brief review and update
2021
·
Natalie Blagowidow
·
American Journal of Medical Genetics Part C Seminars in Medical Genetics
·
11
Clinical, developmental and molecular update on Cornelia de Lange syndrome and the cohesin complex: Abstracts from the 2014 Scientific and Educational Symposium
2015
·
Antonie D. Kline
, Anne L. Calof
, et al.
·
American Journal of Medical Genetics Part A
·
6
Fragile X mutation screening among unselected pregnant women seen for genetic counseling: Findings of a pilot study
1999
·
B. Finucane
, V. Speare
, et al.
·
Genetics in Medicine
·
1
PDF
22q11.2 deletion syndrome: the case for routine prenatal genetic screening
2026
·
Natalie Blagowidow
, Anne S. Bassett
, et al.
·
Frontiers in Medicine
Neurodevelopmental Cases: Cognitive Issues and Tall Stature
2024
·
Natalie Blagowidow
·
Elsevier eBooks
Endocrine and Growth Cases: Small Stature and Delayed Puberty
2024
·
Natalie Blagowidow
·
Elsevier eBooks
Contributors
2024
·
Daniah Albokhari
, Houriya Ayoubieh
, et al.
·
Elsevier eBooks
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Works count:
16
Citation count:
822
H-index:
10
I10-index:
10
Year
Topic
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