Chalhoub, Nader: search on Z-Library

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

1

NT5C2novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup

Mahmoud F. Elsaid,Khalid Ibrahim,Nader Chalhoub,Ahmed Elsotouhy…

Journal:

BMC Medical Genetics

Year:

2017

Language:

english

File:

PDF, 775 KB

english, 2017

2

Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance

Kumar, Pankaj, Al-Shafai, Mashael, Al Muftah, Wadha, Chalhoub, Nader, Elsaid, Mahmoud F, Aleem, Alice, Suhre, Karsten

Journal:

BMC Research Notes

Year:

2014

Language:

english

File:

PDF, 844 KB

english, 2014

3

PTEN and the PI3-Kinase Pathway in Cancer

Chalhoub, Nader, Baker, Suzanne J.

Journal:

Annual Review of Pathology Mechanisms of Disease

Year:

2009

Language:

english

File:

PDF, 1.50 MB

english, 2009

4

Homozygous Nonsense Mutation in SCHIP1/IQCJ-SCHIP1 Causes a Neurodevelopmental Brain Malformation Syndrome

Elsaid, Mahmoud, Chalhoub, Nader, Ben-Omran, Tawfeg, Kamel, Hussein, Al Mureikhi, Mariam, Ibrahim, Khalid, Ross, M. Elizabeth, Abdel Aleem, Alice

Journal:

Clinical Genetics

Year:

2017

Language:

english

File:

PDF, 1.33 MB

english, 2017

5

Genotype analysis of the NF1 gene in the French Canadians from the Québec population

Lijuan Fang, Nader Chalhoub, Wentian Li, Josué Feingold, June Ortenberg, Bernard Lemieux, Jean-Paul Thirion

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 229 KB

english, 2001

6

Severe Malignant Osteopetrosis Caused by a GL Gene Mutation

Paola Quarello, Marco Forni, Laura Barberis, Claudio Defilippi, M Francesca Campagnoli, Leandra Silvestro, Annalisa Frattini, Nader Chalhoub, Jean Vacher, Ugo Ramenghi

Journal:

Journal of Bone and Mineral Research

Year:

2004

Language:

english

File:

PDF, 1.86 MB

english, 2004

7

Mo1741 Sensory Evaluation of Commercial Bowel Cleansing Solutions

Olabi, Ammar A., Georges, Camille A., Daroub, Hamza, Chalhoub, Jean M., Shayto, Rani, Nader, Ralph G., Chaar, Hani F., Sharara, Ala I.

Journal:

Gastroenterology

Year:

2016

Language:

english

File:

PDF, 624 KB

english, 2016

8

Physical and transcriptional map of the mouse Chromosome 10 proximal region syntenic to human 6q16-q21

Nader Chalhoub, Nadia Benachenhou, Jean Vacher

Journal:

Mammalian Genome

Year:

2001

Language:

english

File:

PDF, 1.52 MB

english, 2001

9

Mutation in non-coding RNA, RNU12 causes early-onset cerebellar ataxia

Elsaid, Mahmoud Fawzi, Chalhoub, Nader, Ben-Omran, Tawfeg, Kumar, Pankaj, Kamel, Hussein, Ibrahim, Khalid, Mohamoud, Yasmin, Al-Dous, Eman, Al-Azwani, Iman, Malek, Joel A., Suhre, Karsten, Ross, M. El

Journal:

Annals of Neurology

Year:

2016

Language:

english

File:

PDF, 2.04 MB

english, 2016

10

Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human

Chalhoub, Nader, Benachenhou, Nadia, Rajapurohitam, Venkatesh, Pata, Monica, Ferron, Mathieu, Frattini, Annalisa, Villa, Anna, Vacher, Jean

Journal:

Nature Medicine

Year:

2003

Language:

english

File:

PDF, 527 KB

english, 2003

11

Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec population

Li Juan Fang, Wentian Li, Nader Chalhoub, Josué Feingold, June Ortenberg, Jean-Paul Thirion

Journal:

Annales de Génétique

Year:

2002

Language:

english

File:

PDF, 73 KB

english, 2002

12

CV44 Faux anevrysme de l’aorte abdominale naissant dans un magma ganglionnaire : diagnostic par echo-Doppler et traitement par embolisation

Hachem, K., Nader, L., Chalhoub, B., Smayra, T., Ghossain, M.

Journal:

Journal de Radiologie

Year:

2005

Language:

french

File:

PDF, 623 KB

french, 2005

13

Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum

Elsaid, Mahmoud F., Kamel, Hussein, Chalhoub, Nader, Aziz, Nahla Abdel, Ibrahim, Khalid, Ben-Omran, Tawfeg, George, Binu, Al-Dous, Eman, Mohamoud, Yasmin, Malek, Joel A., Ross, M. Elizabeth, Aleem, Al

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 230 KB

english, 2014

14

Clinical and Genomic characteristics of LAMA2 Related congenital Muscular Dystrophy in a Patientsâ Cohort from Qatar. A population Specific Founder Variant

Aleem, Alice Abdel, Elsaid, Mahmoud F., Chalhoub, Nader, Chakroun, Almahdi, Mohamed, Khalid A.S., AlShami, Rana, Kuzu, Omer, Mohamed, Reem, Ibrahim, Khalid, AlMudheki, Noora, Osman, Omar, Ross, M. Eli

Journal:

Neuromuscular Disorders

Year:

2020

File:

PDF, 2.68 MB

2020

15

S6k1 is not required for Pten-deficient neuronal hypertrophy

Nader Chalhoub, Sara C. Kozma, Suzanne J. Baker

Journal:

Year:

2006

Language:

english

File:

PDF, 872 KB

english, 2006

16

Novel mutations target distinct subgroups of medulloblastoma

Robinson, Giles, Parker, Matthew, Kranenburg, Tanya A., Lu, Charles, Chen, Xiang, Ding, Li, Phoenix, Timothy N., Hedlund, Erin, Wei, Lei, Zhu, Xiaoyan, Chalhoub, Nader, Baker, Suzanne J., Huether, Rob

Journal:

Year:

2012

Language:

english

File:

PDF, 2.02 MB

english, 2012

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