Morrow, Bernice E.: search on Z-Library

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

51

Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects

Sewda, Anshuman, Agopian, A. J., Goldmuntz, Elizabeth, Hakonarson, Hakon, Morrow, Bernice E., Musfee, Fadi, Taylor, Deanne, Mitchell, Laura E., Winlaw, David Scott

Journal:

Year:

2020

File:

PDF, 774 KB

2020

52

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

Davies, Robert W., Fiksinski, Ania M., Breetvelt, Elemi J., Williams, Nigel M., Hooper, Stephen R., Monfeuga, Thomas, Bassett, Anne S., Owen, Michael J., Gur, Raquel E., Morrow, Bernice E., McDonald-M

Journal:

Nature Medicine

Year:

2020

File:

PDF, 1.63 MB

2020

53

The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder

Wenger, Tara L., Kao, Charlly, McDonald-McGinn, Donna M., Zackai, Elaine H., Bailey, Alice, Schultz, Robert T., Morrow, Bernice E., Emanuel, Beverly S., Hakonarson, Hakon

Journal:

Scientific Reports

Year:

2016

Language:

english

File:

PDF, 346 KB

english, 2016

54

Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome

Racedo, Silvia E., Hasten, Erica, Lin, Mingyan, Devakanmalai, Gnanapackiam Sheela, Guo, Tingwei, Ozbudak, Ertugrul M., Cai, Chen-Leng, Zheng, Deyou, Morrow, Bernice E., Barsh, Gregory S.

Journal:

Year:

2017

Language:

english

File:

PDF, 3.36 MB

english, 2017

55

549: Genetic interactions in inner ear development

Mary King, Ingrid Torregroza, Todd Evans, Bernice Morrow

Journal:

American Journal of Obstetrics and Gynecology

Year:

2008

Language:

english

File:

PDF, 94 KB

english, 2008

56

NOTCH maintains developmental cardiac gene network through WNT5A

Wang, Yidong, Lu, Pengfei, Wu, Bingruo, Morrow, Bernice E., Zhou, Bin

Journal:

Journal of Molecular and Cellular Cardiology

Year:

2018

Language:

english

File:

PDF, 1.93 MB

english, 2018

57

Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling

Subreena Simrick, Dorota Szumska, Jennifer R. Gardiner, Kieran Jones, Karun Sagar, Bernice Morrow, Shoumo Bhattacharya, M. Albert Basson

Journal:

Developmental Dynamics

Year:

2012

Language:

english

File:

PDF, 3.03 MB

english, 2012

58

Low-Copy Repeats Mediate the Common 3-Mb Deletion in Patients with Velo-cardio-facial Syndrome

Lisa Edelmann, Raj K. Pandita, Bernice E. Morrow

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 3.35 MB

english, 1999

59

Comparative Mapping of the Human 22q11 Chromosomal Region and the Orthologous Region in Mice Reveals Complex Changes in Gene Organization

Anne Puech, Bruno Saint-Jore, Birgit Funke, Debra J. Gilbert, Howard Sirotkin, Neal G. Copeland, Nancy A. Jenkins, Raju Kucherlapati, Bernice Morrow and Arthur I. Skoultchi

Journal:

Proceedings of the National Academy of Sciences

Year:

1997

Language:

english

File:

PDF, 1.20 MB

english, 1997

60

Integrated rare variant-based risk gene prioritization in disease case-control sequencing studies

Lin, Jhih-Rong, Zhang, Quanwei, Cai, Ying, Morrow, Bernice E., Zhang, Zhengdong D., Zhu, Xiaofeng

Journal:

Year:

2017

Language:

english

File:

PDF, 8.54 MB

english, 2017

61

Velo-cardio-facial syndrome: Frequency and extent of 22q1l deletions

Elizabeth A. Lindsay, Rosalie Goldberg, Vesna Jurecic, Bernice Morrow, Christine Carlson, Raju S. Kucherlapati, Robert J. Shprintzen, Antonio Baldini

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 622 KB

english, 1995

62

Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature

Marilena Petti, Joy Samanich, Qiulu Pan, Chih-Kang Huang, Jana Reinmund, Sadaf Farooqi, Bernice Morrow, Melanie Babcock

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 584 KB

english, 2011

63

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

R. Matsuoka, Misa Kimura, Peter J. Scambler, Bernice E. Morrow, Shin-ichiro Imamura, Shinsei Minoshima, Nobuyoshi Shimizu, Hiroyuki Yamagishi, Kunitaka Joh-o, Seiichi Watanabe, Kotaro Oyama, Tsutomu S

Journal:

Year:

1998

Language:

english

File:

PDF, 519 KB

english, 1998

64

Meiotic Pachytene Arrest in MLH1-Deficient Mice

Winfried Edelmann, Paula E Cohen, Michael Kane, Kirkland Lau, Bernice Morrow, Samuel Bennett, Asad Umar, Thomas Kunkel, Giorgio Cattoretti, Raju Chaganti, Jeffrey W Pollard, Richard D Kolodner, Raju K

Journal:

Year:

1996

Language:

english

File:

PDF, 2.05 MB

english, 1996

65

Mouse and Human CRKL Is Dosage Sensitive for Cardiac Outflow Tract Formation

Racedo, Silvia E., McDonald-McGinn, Donna M., Chung, Jonathan H., Goldmuntz, Elizabeth, Zackai, Elaine, Emanuel, Beverly S., Zhou, Bin, Funke, Birgit, Morrow, Bernice E.

Journal:

The American Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.30 MB

english, 2015

66

Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome

Lachman, Herbert M., Morrow, Bernice, Shprintzen, Robert, Veit, Sabine, Parsia, Sam S., Faedda, Gianni, Goldberg, Rosalie, Kucherlapati, Raju, Papolos, Demitri F.

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 519 KB

english, 1996

67

Tbx1 heterozygosity impairs working memory in mice

Takeshi Hiramoto, Go Suzuki, Gina Kang, Birgit Funke, Yasuhiro Watanabe, Raju Kucherlapati, Bernice Morrow, Noboru Hiroi

Journal:

Neuroscience Research

Year:

2009

Language:

english

File:

PDF, 128 KB

english, 2009

68

Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives

Pulver, Ann E., Nestadt, Gerald, Goldberg, Rosalie, Shprintzen, Robert J., Lamacz, Malgorzata, Wolyniec, Paula S., Morrow, Bernice, Karayiorgou, Maria, Antonarakis, Stylianos E., Housman, David, Kuche

Journal:

Journal of Nervous & Mental Disease

Year:

1994

File:

PDF, 330 KB

1994

69

Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome

Jeffrey M. Long, Patricia LaPorte, Sandra Merscher, Birgit Funke, Bruno Saint-Jore, Anne Puech, Raju Kucherlapati, Bernice E. Morrow, Arthur I. Skoultchi, Anthony Wynshaw-Boris

Journal:

Year:

2006

Language:

english

File:

PDF, 284 KB

english, 2006

70

Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairment

Joy Samanich, Christina Lowes, Robert Burk, Sara Shanske, J. Lu, Alan Shanske, Bernice E. Morrow

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 274 KB

english, 2007

71

Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndrome

Delio, Maria, Pope, Kathleen, Wang, Tao, Samanich, Joy, Haldeman-Englert, Chad R., Kaplan, Paige, Shaikh, Tamim H., Cai, Jinlu, Marion, Robert W., Morrow, Bernice E., Babcock, Melanie

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 611 KB

english, 2013

72

Characterization of the past and current duplication activities in the human 22q11.2 region

Xingyi Guo, Laina Freyer, Bernice Morrow, Deyou Zheng

Journal:

Year:

2011

Language:

english

File:

PDF, 4.41 MB

english, 2011

73

Tbx3 & Tbx15 expression in the limb bud of wild type & Fgf10 knockout mice

Mary King (F), Frank Diaz, Alex Bondarev, Vimla Aggarwal, Alan Shanske, Bernice Morrow

Journal:

American Journal of Obstetrics and Gynecology

Year:

2005

Language:

english

File:

PDF, 57 KB

english, 2005

74

Tbx1 regulates mesenchymal–epithelial signaling necessary for inner ear development

Dennis C. Monks, Evan M. Braunstein, Bernice E. Morrow

Journal:

Developmental Biology

Year:

2009

Language:

english

File:

PDF, 70 KB

english, 2009

75

709: Gene expression profiling of lymphoblastic cell lines from monosomy 1p36 patients reveals differential regulation (expression) of cardiac and neurologic relevant genes

Avishai Alkalay, Melanie Babcock, Anna Bergsmedh, Dennis Monks, Mary E. King, Lisa Shaffer, Bernice Morrow

Journal:

American Journal of Obstetrics and Gynecology

Year:

2009

Language:

english

File:

PDF, 104 KB

english, 2009

76

Agnathia–otocephaly complex: A case report and examination of the OTX2 and PRRX1 genes

Sean Herman, Maria Delio, Bernice Morrow, Joy Samanich

Journal:

Year:

2012

Language:

english

File:

PDF, 326 KB

english, 2012

77

The Role of Neural Crest during Cardiac Development in a Mouse Model of DiGeorge Syndrome

Lazaros Kochilas, Sandra Merscher-Gomez, Min Min Lu, Vijaya Potluri, Jun Liao, Raju Kucherlapati, Bernice Morrow, Jonathan A. Epstein

Journal:

Developmental Biology

Year:

2002

Language:

english

File:

PDF, 645 KB

english, 2002

78

Isolation and Characterization of a Novel Gene Containing WD40 Repeats from the Region Deleted in Velo–cardio–facial/ DiGeorge Syndrome on Chromosome 22q11

Birgit Funke, Raj K. Pandita, Bernice E. Morrow

Journal:

Year:

2001

Language:

english

File:

PDF, 546 KB

english, 2001

79

Genetic evaluation of American minority pediatric cochlear implant recipients

Tova C. Fischer, Joy Samanich, Bernice E. Morrow, Janie Chobot-Rodd, Alan Shanske, Sanjay R. Parikh

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2009

Language:

english

File:

PDF, 232 KB

english, 2009

80

Detection of an Atypical 22q11 Deletion That Has No Overlap with the DiGeorge Syndrome Critical Region

HILARY O'DONNELL, CAROLE MCKEOWN, CLIVE GOULD, BERNICE MORROW, PETER SCAMBLER

Journal:

The American Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 483 KB

english, 1997

81

Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome

Guo, Tingwei, Chung, Jonathan H., Wang, Tao, McDonald-McGinn, Donna M., Kates, Wendy R., Hawuła, Wanda, Coleman, Karlene, Zackai, Elaine, Emanuel, Beverly S., Morrow, Bernice E.

Journal:

The American Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 9.22 MB

english, 2015

82

Schizophrenia Susceptibility Associated with Interstitial Deletions of Chromosome 22q11

Maria Karayiorgou, Michael A. Morris, Bernice Morrow, Robert J. Shprintzen, Rosalie Goldberg, Julian Borrow, Arnaud Gos, Gerald Nestadt, Paula S. Wolyniec, Virginia K. Lasseter, Harvey Eisen, Barton C

Journal:

Proceedings of the National Academy of Sciences

Year:

1995

Language:

english

File:

PDF, 1.06 MB

english, 1995

83

Encyclopedia of Life Sciences || Microdeletions and Microduplications: Mechanism

Morrow, Bernice E

Year:

2001

Language:

english

File:

PDF, 98 KB

english, 2001

84

GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent

Jidong Shan, Janie Chobot-Rodd, Raquel Castellanos, Melanie Babcock, Alan Shanske, Sanjay R. Parikh, Bernice E. Morrow, Joy Samanich

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2010

Language:

english

File:

PDF, 302 KB

english, 2010

85

A Novel, Single Nucleotide Polymorphism-Based Assay to Detect 22q11 Deletions

Funke, Birgit H., Brown, Alison C., Ramoni, Marco F., Regan, Maura E., Baglieri, Chris, Finn, Christine T., Babcock, Melanie, Shprintzen, Robert J., Morrow, Bernice E., Kucherlapati, Raju

Journal:

Genetic Testing

Year:

2007

Language:

english

File:

PDF, 5.16 MB

english, 2007

86

TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome

Corbitt, Holly, Morris, Shaine A., Gravholt, Claus H., Mortensen, Kristian H., Tippner-Hedges, Rebecca, Silberbach, Michael, Maslen, Cheryl L., Morrow, Bernice E

Journal:

Year:

2018

Language:

english

File:

PDF, 2.29 MB

english, 2018

87

Molecular genetics of 22q11.2 deletion syndrome

Morrow, Bernice E., McDonald-McGinn, Donna M., Emanuel, Beverly S., Vermeesch, Joris R., Scambler, Peter J.

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 1.61 MB

english, 2018

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