E-LIB Suche - Ergebnisse für: Sekhon, Gurbax S.

1

Utility of subtelomeric fluorescent DNA probes for detectio..:

Jalal, Syed M. ; Harwood, Aaron R. ; Sekhon, Gurbax S....
Genetics in Medicine. 5 (2003) 1 - p. 28-34 , 2003

2

Ventricular noncompaction and distal chromosome 5q deletion:

Pauli, Richard M. ; Scheib-Wixted, Susan ; Cripe, Linda..
American Journal of Medical Genetics. 85 (1999) 4 - p. 419-423 , 1999

Link: https://doi.org/10.1002/..

3

Detection of Mosaicism in amniotic fluid cultures: A CYT020..:

Ing, Paul S. ; Van Dyke, Daniel L. ; Caudill, Samuel P....
Genetics in Medicine. 1 (1999) 3 - p. 94-97 , 1999

Link: https://doi.org/10.1097/..

4

Detection of 46,XX male by Y-specific whole chromosome pain..:

Jalal, Syed M. ; Law, Mark E. ; Dewald, Gordon W...
American Journal of Medical Genetics. 52 (1994) 2 - p. 239-241 , 1994

Link: https://doi.org/10.1002/..

5

De novo translocation involving chromosomes 1 and 4 resulti..:

Legare, Janet M. ; Sekhon, Gurbax S. ; Laxova, Renata
American Journal of Medical Genetics. 53 (1994) 3 - p. 216-221 , 1994

Link: https://doi.org/10.1002/..

6

Waardenburg syndrome type I in a child with deletion (2) (q..:

Kirkpatrick, Susan J. ; Kent, Christine M. ; Laxova, Renata.
American Journal of Medical Genetics. 44 (1992) 5 - p. 699-700 , 1992

Link: https://doi.org/10.1002/..

7

Terminal deletion of 6q and Fryns syndrome: A microdeletion..:

Krassikoff, Natalie ; Sekhon, Gurbax S.
American Journal of Medical Genetics. 36 (1990) 3 - p. 363-364 , 1990

Link: https://doi.org/10.1002/..

8

Gene complementing xeroderma pigmentosum group A cells maps..:

Henning, Karla A. ; Schultz, Roger A. ; Sekhon, Gurbax S..
Somatic Cell and Molecular Genetics. 16 (1990) 4 - p. 395-400 , 1990

Link: https://doi.org/10.1007/..

9

Familial agnathia‐holoprosencephaly caused by an inherited ..:

Krassikoff, Natalie ; Sekhon, Gurbax S.
American Journal of Medical Genetics. 34 (1989) 2 - p. 255-257 , 1989

Link: https://doi.org/10.1002/..

10

Mapping of prolactin and tumor necrosis factor-beta genes o..:

Evans, Alida M. ; Petersen, Jean W. ; Sekhon, Gurbax S..
Somatic Cell and Molecular Genetics. 15 (1989) 3 - p. 203-213 , 1989

Link: https://doi.org/10.1007/..

11

Recent experience in prenatal fra(X) detection:

Jenkins, Edmund C. ; Brown, W. Ted ; Krawczun, Michael S....
American Journal of Medical Genetics. 30 (1988) 1-2 - p. 329-336 , 1988

Link: https://doi.org/10.1002/..

12

Mosaic isochromosome 12p:

Pauli, Richard M. ; Zeier, Renee A. ; Sekhon, Gurbax S..
American Journal of Medical Genetics. 27 (1987) 2 - p. 291-294 , 1987

Link: https://doi.org/10.1002/..

13

Interstitial deletion of (17)(p11.2p11.2): Report of six ad..:

Stratton, Robert F. ; Dobyns, William B. ; Greenberg, Frank...
American Journal of Medical Genetics. 24 (1986) 3 - p. 421-432 , 1986

Link: https://doi.org/10.1002/..

14

A new syndrome of proximal deletion of the long arm of chro..:

Taysi, Kutay ; Sekhon, Gurbax S. ; Hillman, Richard E..
American Journal of Medical Genetics. 13 (1982) 4 - p. 423-430 , 1982

Link: https://doi.org/10.1002/..

15

Concordant congenital malformations in twins with inherited..:

Sekhon, Gurbax S. ; Taysi, Kutay
Human Genetics. 50 (1979) 3 - p. 271-276 , 1979

Link: https://doi.org/10.1007/..