Arthur C. Grix: search on Z-Library

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1

Absence of malignant hyperthermia contractures in Becker-Duchenne dystrophy at age 2

Dr. Gerald A. Gronert, Dr. William Fowler, Dr. George H. Cardinet III, Dr. Arthur Grix Jr., Dr. William G. Ellis, Dr. Marshall Z. Schwartz

Journal:

Year:

1992

Language:

english

File:

PDF, 638 KB

english, 1992

2

Diagnostic criteria for Walker-Warburg syndrome

William B. Dobyns, Roberta A. Pagon, Dawna Armstrong, Cynthia J. R. Curry, Frank Greenberg, Arthur Grix, Lewis B. Holmes, Renata Laxova, Virginia V. Michels, Meinhard Robinow, Roberta L. Zimmerman, Jo

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 1.59 MB

english, 1989

3

Interstitial deletion of the short arm of chromosome 1 (46XY), del(1)(p13p22.3)

Frank R. Mattia, Terrance D. Wardinsky, Deborah J. Tuttle, Arthur Grix Jr., Kathleen A. Smith, Paula Walling

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 323 KB

english, 1992

4

Pleiotropy in Coffin-Lowry syndrome: Sensorineural hearing deficit and premature tooth loss as early manifestations

James K. Hartsfield Jr., Bryan D. Hall, Arthur W. Grix, Boris G. Kousseff, Jose F. Salazar, Scott M. W. Haufe

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 1.19 MB

english, 1993

5

Reply to Dr. Köhler

Arthur Grix, Paula Walling, Terrance D. Wardinsky

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 55 KB

english, 1993

6

A tribute to Bryan D. Hall: Festschrift 2003

John C. Carey, Cynthia J.R. Curry, Arthur W. Grix, Mahin Golabi, John M. Graham Jr, Bruce A. Buehler

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 92 KB

english, 2003

7

Frontometaphyseal dysplasia: Mutations in FLNA and phenotypic diversity

Stephen P. Robertson, Zandra A. Jenkins, Timothy Morgan, Lesley Adès, Salim Aftimos, Odile Boute, Torunn Fiskerstrand, Sixto Garcia-Miñaur, Arthur Grix, Andrew Green, Vazken Der Kaloustian, Ray Lewkon

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 246 KB

english, 2006

8

Frontometaphyseal dysplasia: Mutations in FLNA and phenotypic diversity (Am J Med Genet 140A: 1726–1736)

Stephen P. Robertson, Zandra A. Jenkins, Timothy Morgan, Lesley Adès, Salim Aftimos, Odile Boute, Torunn Fiskerstrand, Sixto Garcia-Miñaur, Arthur Grix, Andrew Green, Vazken Der Kaloustian, Ray Lewkon

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 57 KB

english, 2006

9

Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome

Diane Beysen, Sarah De Jaegere, David Amor, Philippe Bouchard, Sophie Christin-Maitre, Marc Fellous, Philippe Touraine, Arthur W. Grix, Raoul Hennekam, Françoise Meire, Nina Oyen, Louise C. Wilson, Da

Journal:

Year:

2008

Language:

english

File:

PDF, 1.05 MB

english, 2008

10

Arthrogryposis multiplex congenita: Prenatal ultrasonographic diagnosis

David P. Gorczyca, John P. McGahan, Karen K. Lindfors, William G. Ellis, Arthur Grix

Journal:

Journal of Clinical Ultrasound

Year:

1989

Language:

english

File:

PDF, 406 KB

english, 1989

11

Prenatal diagnosis of lissencephaly: Miller-Dieker syndrome

John P. McGahan, Arthur Grix, Eugenio O. Gerscovich

Journal:

Journal of Clinical Ultrasound

Year:

1994

Language:

english

File:

PDF, 428 KB

english, 1994

12

Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting

Irfan Saadi, Fowzan S. Alkuraya, Stephen S. Gisselbrecht, Wolfram Goessling, Resy Cavallesco, Annick Turbe-Doan, Aline L. Petrin, James Harris, Ursela Siddiqui, Arthur W. Grix Jr., Hanne D. Hove, Phil

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 2.41 MB

english, 2011

13

Dyskeratosis Congenita Associated with Elevated Fetal Hemoglobin, X-Linked Ocular Albinism, and Juvenile-Onset Diabetes Mellitus

Martin Reichel, Arthur C. Grix, R. Rivkah Isseroff

Journal:

Pediatric Dermatology

Year:

1992

Language:

english

File:

PDF, 817 KB

english, 1992

14

OA1 Mutations and Deletions in X-Linked Ocular Albinism

Rhonda E. Schnur, Mei Gao, Penelope A. Wick, Margaret Keller, Paul J. Benke, Matthew J. Edwards, Arthur W. Grix, Athel Hockey, Jack H. Jung, Kenneth K. Kidd, Mildred Kistenmacher, Alex V. Levin, Richa

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 234 KB

english, 1998

15

A Locus for Bilateral Perisylvian Polymicrogyria Maps to Xq28

Laurent Villard, Karine Nguyen, Carlos Cardoso, Christa Lese Martin, Ann M. Weiss, Mara Sifry-Platt, Arthur W. Grix, John M. Graham Jr, Robin M. Winter, Richard J. Leventer, William B. Dobyns

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 1.04 MB

english, 2002

16

Focal dermal hypoplasia: Four cases with widely varying presentations

Suzanne Linsmeier Kilmer, Arthur W. Grix Jr., R. Rivkah Isseroff

Journal:

Journal of the American Academy of Dermatology

Year:

1993

Language:

english

File:

PDF, 2.44 MB

english, 1993

17

Direct prenatal chromosome diagnosis of a malignancy

Frederick Hecht, Arthur Grix Jr., Barbara K. Hecht, Carol Berger, Helen Bixenman, Susan Szucs, Daniel O'Keeffe, Harris J. Finberg

Journal:

Cancer Genetics and Cytogenetics

Year:

1984

Language:

english

File:

PDF, 264 KB

english, 1984