🐜
|
Twenty-eight loci form a continuous linkage map of markers for human chromosome 1.
8 auth.
P. O'Connell,
G. Lathrop,
Y. Nakamura,
M. Leppert,
R. Ardinger,
J. Murray,
...
J. Lalouel,
R. White
|
6 |
1989 |
6 🐜
|
🐬
|
Cardiovascular malformations in Smith-Lemli-Opitz syndrome.
A. Lin,
H. Ardinger,
R. Ardinger,
C. Cunniff,
R. Kelley
|
6 |
1997 |
6 🐬
|
🐬
|
Evaluation of remote stethoscopy for pediatric telecardiology.
J. Belmont,
L. Mattioli,
K. Goertz,
R. Ardinger,
C. Thomas
|
5 |
1995 |
5 🐬
|
🦁
|
Cerebrovascular stenoses with cerebral infarction in a child with Williams syndrome.
R. Ardinger,
K. Goertz,
L. Mattioli
|
4 |
1994 |
4 🦁
|
🐜
|
Linkage analysis of autosomal dominant atrio ventricular canal defects: exclusion of chromosome 21
7 auth.
A. Cousineau,
R. Lauer,
M. Pierpont,
T. Burns,
R. Ardinger,
S. Patil,
...
V. Sheffield
|
4 |
1994 |
4 🐜
|
🐬
|
Pediatric cardiology: auscultation from 280 miles away.
L. Mattioli,
K. Goertz,
R. Ardinger,
J. Belmont,
R. Cox,
C. Thomas
|
4 |
1992 |
4 🐬
|
🐬
|
RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19.
H. Ardinger,
R. Ardinger,
G. Bell,
J. Murray
|
3 |
1988 |
3 🐬
|
🦁
|
Genetic counseling in congenital heart disease.
R. Ardinger
|
2 |
1997 |
2 🦁
|