Sekhon, Gurbax S: search on Z-Library

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1

Waardenburg syndrome type I in a child with deletion (2) (q35q36.2)

Susan J. Kirkpatrick, Christine M. Kent, Renata Laxova, Gurbax S. Sekhon

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 204 KB

english, 1992

2

Gene complementing xeroderma pigmentosum group A cells maps to distal human chromosome 9q

Karla A. Henning, Roger A. Schultz, Gurbax S. Sekhon, Errol C. Friedberg

Journal:

Somatic Cell and Molecular Genetics

Year:

1990

Language:

english

File:

PDF, 513 KB

english, 1990

3

Ventricular noncompaction and distal chromosome 5q deletion

Pauli, Richard M., Scheib-Wixted, Susan, Cripe, Linda, Izumo, Seigo, Sekhon, Gurbax S.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 666 KB

english, 1999

4

Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q-;6p+)

Kutay Taysi, Gurbax Singh Sekhon

Journal:

Year:

1978

Language:

english

File:

PDF, 447 KB

english, 1978

5

Concordant congenital malformations in twins with inherited translocation: t(9p-;13q+)

Gurbax S. Sekhon, Kutay Taysi

Journal:

Year:

1979

Language:

english

File:

PDF, 1.10 MB

english, 1979

6

Partial trisomy for the short arm of chromosome 2 due to familial balanced translocation

Gurbax Singh Sekhon, Kutay Taysi, Richard Rath

Journal:

Year:

1978

Language:

english

File:

PDF, 234 KB

english, 1978

7

An XX male: Cytogenetic and endocrine studies

Maria E. Rios, Robert L. Kaufman, Gurbax S. Sekhon, James G. Bucy, Joan E. Bauman, Lawrence S. Jacobs

Journal:

Clinical Genetics

Year:

1975

Language:

english

File:

PDF, 556 KB

english, 1975

8

Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients

Jalal, Syed M, Harwood, Aaron R, Sekhon, Gurbax S, Lorentz, Cindy Pham, Ketterling, Rhett P, Babovic-Vuksanovic, Dusica, Meyer, Reid G, Ensenauer, Regina, Anderson, Marvin H, Michels, Virginia V

Journal:

Genetics in Medicine

Year:

2003

Language:

english

File:

PDF, 1.73 MB

english, 2003

9

Delineation of two distinct 6p deletion syndromes

Angela F. Davies, Ghazala Mirza, Gurbax Sekhon, Peter Turnpenny, Frank Leroy, Frank Speleman, Caroline Law, Nicole van Regemorter, Esther Vamos, Frances Flinter, J. Ragoussis

Journal:

Year:

1999

Language:

english

File:

PDF, 412 KB

english, 1999

10

A male infant with Xq22.2q22.3 duplication containing PLP1 and MID2

Chanchani, Swati R., Xie, Hongyan, Sekhon, Gurbax, Melikishvili, Ana M., Moyer Harasink, Sue, Pall, Harpreet, Giampietro, Philip F.

Journal:

Molecular Genetics & Genomic Medicine

Year:

2020

File:

PDF, 622 KB

2020

11

Detection of 46,XX male by Y-specific whole chromosome paint probe

Dr. Syed M. Jalal, Mark E. Law, Gordon W. Dewald, Gurbax S. Sekhon, Daniel L. Van Dyke

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 209 KB

english, 1994

12

Monosomy 18q 12.1→21.1: A recognizable aneuploidy syndrome? Report of a patient and review of the literature

Dr. Natalie Krasikov, Kate Thompson, Gurbax Singh Sekhon

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 412 KB

english, 1992

13

Del(10)(q22.3q24.1) associated with juvenile polyposis

Jacoby, Russell F., Schlack, Steven, Sekhon, Gurbax, Laxova, Renata

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 178 KB

english, 1997

14

Mapping of prolactin and tumor necrosis factor-beta genes on human chromosome 6p using lymphoblastoid cell deletion mutants

Alida M. Evans, Jean W. Petersen, Gurbax S. Sekhon, Robert DeMars

Journal:

Somatic Cell and Molecular Genetics

Year:

1989

Language:

english

File:

PDF, 1.30 MB

english, 1989

15

Recent experience in prenatal fra(X) detection

Edmund C. Jenkins, W. Ted Brown, Michael S. Krawczun, Charlotte J. Duncan, Kusum P. Lele, Eduardo S. Cantu, Steven Schonberg, Mitchell S. Golbus, Gurbax S. Sekhon, Sandra Stark, Suphat Kunaporn, Wayne

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 393 KB

english, 1988

16

A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21–23→1q25

Kutay Taysi, Gurbax S. Sekhon, Richard E. Hillman, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1982

Language:

english

File:

PDF, 417 KB

english, 1982

17

Pathological Case of the Month

Costakos, Dennis T., Love, Laureen A., Josephson, Kevin, Sekhon, Gurbax

Journal:

Archives of Pediatrics and Adolescent Medicine

Year:

1998

File:

PDF, 291 KB

1998

18

De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p

Janet M. Legare, Gurbax S. Sekhon, Renata Laxova

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 525 KB

english, 1994

19

Derepression ofHPRTlocus on inactive X chromosome of human lymphoblastoid cell line

Nancy Nadon, Gurbax Sekhon, Laura J. Brown, Nancy Korn, Jean W. Petersen, Joan Strandtmann, Cecile Chang, Robert DeMars

Journal:

Somatic Cell and Molecular Genetics

Year:

1986

Language:

english

File:

PDF, 1.86 MB

english, 1986

20

Familial agnathia-holoprosencephaly caused by an inherited unbalanced translocation and not autosomal recessive inheritance

Natalie Krassikoff, Gurbax S. Sekhon

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 197 KB

english, 1989

21

Mosaic isochromosome 12p

Richard M. Pauli, Renee A. Zeier, Gurbax S. Sekhon, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 550 KB

english, 1987

22

Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: Localization to Xq27.3-qter

Gregg, Ronald G., Metzenberg, Aida B., Hogan, Kirk, Sekhon, Gurbax, Laxova, Renata

Journal:

Year:

1991

Language:

english

File:

PDF, 601 KB

english, 1991

23

Permanent Lymphoid Lines from Genetically Marked Lymphocytes: Success with Lymphocytes Recovered from Frozen Storage

William S. Sly, Gurbax Singh Sekhon, Roger Kennett, Walter F. Bodmer, Julia Bodmer

Journal:

Tissue Antigens

Year:

1976

Language:

english

File:

PDF, 516 KB

english, 1976

24

Interstitial deletion of (17)(p11.2p11.2): Report of six additional patients with a new chromosome deletion syndrome

Robert F. Stratton, William B. Dobyns, Frank Greenberg, Jeanne B. DeSana, Charleen Moore, George Fidone, Gretchen H. Runge, Paula Feldman, Gurbax S. Sekhon, Richard M. Pauli, Dr. David H. Ledbetter, J

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 913 KB

english, 1986

25

Absence of predictable phenotypic expression in proximal 15q duplications

Carol J. Ludowese, Kate J. Thompson, Gurbax S. Sekhon, Richard M. Pauli

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 547 KB

english, 1991

26

Terminal deletion of 6q and Fryns syndrome: A microdeletion/syndrome pair?

Natalie Krassikoff, Gurbax S. Sekhon

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 236 KB

english, 1990

27

Application of Multicolor Fluorescent In Situ Hybridization for Enhanced Characterization of Chromosomal Abnormalities in Congenital Disorders

Jalal, Syed M., Law, Mark E., Lindor, Noralane M., Thompson, Kate J., Sekhon, Gurbax S.

Journal:

Mayo Clinic Proceedings

Year:

2001

Language:

english

File:

PDF, 239 KB

english, 2001

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