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Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms
96 auth.
M. Kaur,
J. Blair,
B. Devkota,
Sierra Fortunato,
Dinah Clark,
Audrey Lawrence,
Wonwook Do,
Benjamin Semeo,
Olivia L. Katz,
D. Mehta,
Nobuko Yamamoto,
Emma A Schindler,
Zayd Al Rawi,
Nina Wallace,
Jonathan J. Wilde,
...
Jennifer McCallum,
Jinglan Liu,
Dongbin Xu,
M. Jackson,
Stefan Rentas,
A. A. Tayoun,
Zhang Zhe,
Omar Abdul-Rahman,
Bill Allen,
Moris A Angula,
K. Anyane-Yeboa,
J. Argente,
P. Arn,
L. Armstrong,
L. Basel-Salmon,
G. Baynam,
L. Bird,
D. Bruegger,
G. Ch'ng,
D. Chitayat,
Robin Clark,
G. Cox,
U. Dave,
Elfrede DeBaere,
M. Field,
J. Graham,
K. Gripp,
R. Greenstein,
Neerja Gupta,
R. Heidenreich,
J. Hoffman,
R. Hopkin,
K. Jones,
Marilyn C. Jones,
A. Kariminejad,
J. Kogan,
B. Lāce,
Julian Leroy,
S. Lynch,
M. McDonald,
Kirsten Meagher,
N. Mendelsohn,
I. Micule,
J. Moeschler,
S. Nampoothiri,
K. Ohashi,
C. Powell,
Subhadra Ramanathan,
S. Raskin,
E. Roeder,
M. Rio,
A. Rope,
Karan Sangha,
A. Scheuerle,
A. Schneider,
S. Shalev,
V. Siu,
Rosemarie Smith,
C. Stevens,
T. Tkemaladze,
John Toimie,
H. Toriello,
A. Turner,
P. Wheeler,
S. White,
T. Young,
K. Loomes,
Mary Pipan,
A. Harrington,
E. Zackai,
R. Rajagopalan,
L. Conlin,
M. Deardorff,
D. McEldrew,
J. Pié,
F. Ramos,
A. Musio,
A. Kline,
K. Izumi,
S. Raible,
I. Krantz
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2023 |
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