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1 .
8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients
저자
by
Sara Ellingwood
;
Wendy E. Smith
;
John C K Barber
;
Arayamparambil C. Anilkumar
;
Yara Kharbutli
, et al.
소스
American Journal of Medical Genetics Part A
. 161:487-500
Web of Science
Scopus
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7 .
Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities
저자
by
Aaron Theisen
;
Dennis Bartholomew
;
Kim L. McBride
;
Wendy E. Smith
;
Jean P. Pfotenhauer
, et al.
소스
The American Journal of Human Genetics
. 86:454-461
Full Text (ScienceDirect O/A)
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7 .
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
저자
by
Beatrice N. French
;
Blake C. Ballif
;
Jill A. Rosenfeld
;
Santhosh Girirajan
;
Eric Haan
, et al.
소스
Nature genetics, vol 42, iss 3
Girirajan, S; Rosenfeld, JA; Cooper, GM; Antonacci, F; Siswara, P; Itsara, A; et al.(2010). A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nature Genetics, 42(3), 203-209. doi: 10.1038/ng.534. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/89w1x55x
Nature genetics
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7 .
Isolation, characterization, and chondrogenic potential of human bone marrow-derived multipotential stromal cells
저자
by
Manas K. Majumdar
;
Elisabeth A. Morris
;
Diane Peluso
;
Valerie Banks
.
소스
Journal of Cellular Physiology
. 185:98-106
Full Text (Wiley)
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6 .
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats
저자
by
Jill A. Rosenfeld
;
Marwan Shinawi
;
Scott Saunders
;
Livija Medne
;
Shashikant Kulkarni
, et al.
소스
Human Mutation, vol. 33, no. 1, pp. 165-179
Open Access (OpenAIRE)
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7 .
Further clinical and molecular delineation of the 15q24 microdeletion syndrome
저자
by
Jill A. Rosenfeld
;
David J. Amor
;
Wendy E. Smith
;
Rosemarie Smith
;
Allen N. Lamb
, et al.
소스
Journal of medical genetics, 49(2), 110-118. BMJ Publishing Group
Journal of Medical Genetics
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7 .
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes
저자
by
Bassem A. Bejjani
;
Anne Chun Hui Tsai
;
Wendy E. Smith
;
Beatrice N. French
;
Jill A. Rosenfeld
, et al.
소스
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7 .
Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25
저자
by
Brad Angle
;
Maria L. Helgeson
;
Ralph S. Lachman
;
Dmitriy Niyazov
;
Wendy E. Smith
, et al.
소스
American journal of medical genetics. Part A
. (6)
Open Access (OpenAIRE)
Scopus
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7 .
Comparing hydrocolloid dressings in management of exuding wounds
저자
by
Sue Hagelstein
;
Valerie Banks
;
Keith G Harding
;
S Bale
;
Nicola Thomas
.
소스
British journal of nursing (Mark Allen Publishing)
. 8(10)
Scopus
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