Proud, Virginia: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Polyhydramnios, fetal overgrowth, and macrocephaly: Prenatal ultrasound findings of Costello syndrome

Laura P. Smith, John Podraza, Virginia K. Proud

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 416 KB

english, 2009

2

Unique family with Townes-Brocks syndrome, SALL1 mutation, and cardiac defects

Winn S. Surka, Juergen Kohlhase, Cindy E. Neunert, Daniel S. Schneider, Virginia K. Proud

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 513 KB

english, 2001

3

Family study of the inheritance of pectus excavatum

Heather A. Creswick, Michael W. Stacey, Robert E. Kelly Jr, Tina Gustin, Donald Nuss, Helen Harvey, Michael J. Goretsky, Ellen Vasser, J. Camille Welch, Karen Mitchell, Virginia K. Proud

Journal:

Journal of Pediatric Surgery

Year:

2006

Language:

english

File:

PDF, 423 KB

english, 2006

4

Molecular aspects, clinical aspects and possible treatment modalities for Costello syndrome: Proceedings from the 1st International Costello Syndrome Research Symposium 2007

Katherine A. Rauen, Erin Hefner, Kristin Carrillo, Jill Taylor, Laure Messier, Yoko Aoki, Karen W. Gripp, Yoichi Matsubara, Virginia K. Proud, Peter Hammond, Judith E. Allanson, Marie-Ange Delrue, Mar

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 130 KB

english, 2008

5

Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocation

Lori L. Bassett, Ron C. Michaelis, Mary Holland Geiger, Jack Tarleton, C. Lynn Moore, Judith F. Knops, Andrew J. Carroll, Virginia K. Proud

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 33 KB

english, 2001

6

Further delineation of cardiac abnormalities in Costello syndrome

Angela E. Lin, Paul D. Grossfeld, Robert M. Hamilton, Leslie Smoot, Karen W. Gripp, Virginia Proud, Rosanna Weksberg, Patricia Wheeler, Jonathan Picker, Mira Irons, Elaine Zackai, Bradley Marino, Char

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 133 KB

english, 2002

7

Adrenoleukodystrophy: Dietary oleic acid lowers hexacosanoate levels

William B. Rizzo, Mary W. Phillips, Andrea L. Dammann, Robert T. Leshner, Sandra S. Jennings, Joel Avigan, Virginia K. Proud

Journal:

Annals of Neurology

Year:

1987

Language:

english

File:

PDF, 758 KB

english, 1987

8

Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III)

Weaver, David D., Norby, Audrey R., Rosenfeld, Jill A., Proud, Virginia K., Spangler, Brooke E., Ming, Jeffrey E., Chisholm, Elizabeth, Zackai, Elaine H., Lee, Beom Hee, Edelmann, Lisa, Desnick, Rober

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 1.45 MB

english, 2015

9

Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus

Kaler, Stephen G., Gallo, Linda K., Proud, Virginia K., Percy, Alan K., Mark, Yvonne, Segal, Neil A., Goldstein, David S., Holmes, Courtney S., Gahl, William A.

Journal:

Nature Genetics

Year:

1994

File:

PDF, 946 KB

1994

10

Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene

Stuart W. Tompson, Carlos A. Bacino, Nicole P. Safina, Michael B. Bober, Virginia K. Proud, Tara Funari, Michael F. Wangler, Lisette Nevarez, Leena Ala-Kokko, William R. Wilcox, David R. Eyre, Deborah

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 487 KB

english, 2010

11

Minimal evidence for a direct involvement of twisted gastrulation homolog 1 (TWSG1) gene in human holoprosencephaly

Emily F. Kauvar, Ping Hu, Daniel E. Pineda-Alvarez, Benjamin D. Solomon, Amalia Dutra, Evgenia Pak, Brooke Blessing, Virginia Proud, Alan L. Shanske, Cathy A. Stevens, Jill A. Rosenfeld, Lisa G. Shaff

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 1.20 MB

english, 2011

12

Distinctive Menkes disease variant with occipital horns: Delineation of natural history and clinical phenotype

Proud, Virginia K., Mussell, Holly G., Kaler, Stephen G., Young, Daniel W., Percy, Alan K.

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 852 KB

english, 1996

13

Updating McKusick: An educational exercise for medical students

MD Joann N. Bodurtha, J. Ives Townsend, Virginia K. Proud, Walter E. Nance, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 577 KB

english, 1986

14

Purification and phosphorylation of initiation factor eIF-2 from rabbit skeletal muscle

Christopher G. Proud, Virginia M. Pain

Journal:

Year:

1982

Language:

english

File:

PDF, 499 KB

english, 1982

15

Hemoglobin Columbia Missouri or α2[88 (F9) Ala→Val]β2: A New High-Oxygen-Affinity Hemoglobin That Causes Erythrocytosis

PERRY, MICHAEL C., HEAD, CHARLOTTE, FAIRBANKS, VIRGIL F., JONES, RICHARD T., TAYLOR, HENRY, PROUD, VIRGINIA

Journal:

Mayo Clinic Proceedings

Year:

1991

Language:

english

File:

PDF, 713 KB

english, 1991

16

Prenatal mucolipidosis type II (I-cell disease) can present as Pacman dysplasia

Robert A. Saul, Virginia Proud, Harold A. Taylor, Jules G. Leroy, Jurgen Spranger

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 189 KB

english, 2005

17

Role of the pediatric otolaryngologist in diagnosis and management of children with mucopolysaccharidoses

Stephen M. Wold, Craig S. Derkay, David H. Darrow, Virginia Proud

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2010

Language:

english

File:

PDF, 352 KB

english, 2010

18

Classification of the dysmorphology of pectus excavatum

Mark J. Cartoski, Donald Nuss, Michael J. Goretsky, Virginia K. Proud, Daniel P. Croitoru, Tina Gustin, Karen Mitchell, Ellen Vasser, Robert E. Kelly Jr.

Journal:

Journal of Pediatric Surgery

Year:

2006

Language:

english

File:

PDF, 8.30 MB

english, 2006

19

Clinical Comparison of Overlapping Deletions of 19p13.3

Risheg, Hiba, Pasion, Romela, Sacharow, Stephanie, Proud, Virginia, Immken, LaDonna, Schwartz, Stuart, Tepperberg, Jim H., Papenhausen, Peter, Tan, Tiong Y., Andrieux, Joris, Plessis, Ghislaine, Amor,

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 314 KB

english, 2013

20

Developmental-Behavioral Pediatrics || GENETIC SYNDROMES AND DYSMORPHOLOGY

Proud, Virginia Kent

Year:

2009

Language:

english

File:

PDF, 1.54 MB

english, 2009

21

Additional EFNB1 mutations in craniofrontonasal syndrome

Deeann Wallis, Felicitas Lacbawan, Mahim Jain, Vazken M. Der Kaloustian, Carlos E. Steiner, John B. Moeschler, H. Wolfgang Losken, Ilkka I. Kaitila, Stephen Cantrell, Virginia K. Proud, John C. Carey,

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 110 KB

english, 2008

22

Regulation of binding of initiator tRNA to eukaryotic initiation factor eIF-2: Effects of the haem-controlled repressor on the kinetics of ternary complex formation

Christopher G. Proud, Michael J. Clemens, Virginia M. Pain

Journal:

Year:

1982

Language:

english

File:

PDF, 738 KB

english, 1982

23

763 THE CURRICULARIZATION OF McKUSICK: AN INNOVATION IN MEDICAL EDUCATION

Bodurtha, Joann N, Townsend, J Ives, Proud, Virginia K, Nance, Walter E, Wolf, B

Journal:

Pediatric Research

Year:

1985

Language:

english

File:

PDF, 162 KB

english, 1985

24

Differences in ribosome-bound and ribosome-free initiation-factor eIF-2 activities from haemin-deficient and haemin-supplemented reticulocyte lysates

PROUD, CHRISTOPHER G., PAIN, VIRGINIA M.

Journal:

Biochemical Society Transactions

Year:

1982

Language:

english

File:

PDF, 119 KB

english, 1982

25

Biochemical changes in temperature-activated statoblasts of an ectoproct bryozoan

Robert E. Black, Virginia K. Proud

Journal:

Journal of Experimental Zoology Part A Ecological Genetics and Physiology

Year:

1976

Language:

english

File:

PDF, 248 KB

english, 1976

26

Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome

Kazuhiko Nakabayashi, Bridget A. Fernandez, Ikuko Teshima, Cheryl Shuman, Virginia K. Proud, Cynthia J. Curry, David Chitayat, Theresa Grebe, Jeffrey Ming, Mitsuo Oshimura, Makiko Meguro, Kohzoh Mitsu

Journal:

Year:

2002

Language:

english

File:

PDF, 1.13 MB

english, 2002

27

Bifid epiglottis and polydactyly: A new genetic syndrome

JOHN E. McCLAY, BRIAN WIATRAK, VIRGINIA K. PROUD

Journal:

Otolaryngology - Head and Neck Surgery

Year:

1997

Language:

english

File:

PDF, 2.89 MB

english, 1997

28

Hardikar syndrome: New features

J. Rainer Poley, Virginia K. Proud

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 279 KB

english, 2008

29

Medical students using Grateful Med: Analysis of failed searches and a six-month follow-up study

Joyce A. Mitchell, E.Diane Johnson, John E. Hewett, Virginia K. Proud

Journal:

Computers and Biomedical Research

Year:

1992

Language:

english

File:

PDF, 855 KB

english, 1992

30

CNS malformation in a child with Kabuki (Niikawa-Kuroki) syndrome: Report and review

Chu, Da-Chang, Finley, Sara C., Young, Daniel W., Proud, Virginia K.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 205 KB

english, 1997

31

Weaver syndrome: Autosomal dominant inheritance of the disorder

Proud, Virginia K., Braddock, Stephen R., Cook, Lola, Weaver, David D.

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 263 KB

english, 1998

32

Pacman dysplasia: a lethal skeletal dysplasia with variable radiographic features

Stephen F. Miller, Virginia K. Proud, Alice L. Werner, Fiona M. Field, William F. Wilcox, Ralph S. Lachman, David L. Rimoin

Journal:

Pediatric Radiology

Year:

2003

Language:

english

File:

PDF, 272 KB

english, 2003

33

Avoiding Transmitting Identified Mutations to Offspring Using Preimplantation Genetic Diagnosis

Smith, Laura P., Hughes, Mark R., Thirumoorthi, Ilango, Proud, Virginia K., Penzias, Alan S.

Journal:

Obstetrics & Gynecology

Year:

2010

Language:

english

File:

PDF, 104 KB

english, 2010

34

Enzyme Replacement Therapy in the Home Setting for Mucopolysaccharidosis VI

Tifft, Cynthia, Proud, Virginia, Levy, Paul, DeMarco, Kristin, Nicely, Helen, Turbeville, Sean

Journal:

Journal of Infusion Nursing

Year:

2009

Language:

english

File:

PDF, 2.29 MB

english, 2009

35

Response to Feingold's: The use of inappropriate, demeaning, and perjorative terminology to describe syndromes

Robert A. Saul, Harold A. Taylor, Jules Leroy, Jurgen Spranger, Virginia Proud

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 50 KB

english, 2006

36

New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum

Virginia K. Proud, Clive Levine, Nancy J. Carpenter

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 812 KB

english, 1992

37

Clinical Findings in Four Children with Biotinidase Deficiency Detected through a Statewide Neonatal Screening Program

Wolf, Barry, Heard, Gregory S., Jefferson, Linda G., Proud, Virginia K., Nance, Walter E., Weissbecker, Karen A.

Journal:

Boston Medical and Surgical Journal

Year:

1985

Language:

english

File:

PDF, 806 KB

english, 1985

38

Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8

Reha M. Toydemir, Harold Chen, Virginia K. Proud, Rick Martin, Hans van Bokhoven, Ben C. J. Hamel, Joep H. Tuerlings, Constantine A. Stratakis, Lynn B. Jorde, Michael J. Bamshad

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 302 KB

english, 2006

39

Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome

David Monk, Emma L Wakeling, Virginia Proud, Megan Hitchins, Sayeda N. Abu-Amero, Philip Stanier, Michael A. Preece, Gudrun E Moore

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 1.07 MB

english, 2000

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски