✦ LIBER ✦

Mo1952 Phenotypic and Genotypic Identification of Campylobacters in Diarrheal Patients and Poultry in and Around Chandigarh, India

✍ Scribed by Vaishnavi, Chetana; Singh, Meenakshi; Thapa, Babu R.

Book ID: 123205295
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 473 KB
Volume: 146
Category: Article
ISSN: 0016-5085
DOI: 10.1016/S0016-5085(14)62542-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Phenotypes and genotypes of campylobacte

Phenotypes and genotypes of campylobacter strains isolated after cleaning and disinfection in poultry slaughterhouses

✍ M.B. Peyrat; C. Soumet; P. Maris; P. Sanders 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 569 KB

Identification of 16 novel mutations in

Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype–phenotype correlation in 38 classical citrullinemia patients

✍ Hong-Zhi Gao; Keiko Kobayashi; Ayako Tabata; Hideaki Tsuge; Mikio Iijima; Tomots 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 195 KB

Classical citrullinemia (CTLN1), a rare autosomal recessive disorder, is caused by mutations of the argininosuccinate synthetase (ASS) gene, localized on chromosome 9q34.1. ASS functions as a rate-limiting enzyme in the urea cycle. Previously, we identified 32 mutations in the ASS gene of CTLN1 pati

Identification of WASP mutations, mutati

Identification of WASP mutations, mutation hotspots and genotype-phenotype disparities in 24 patients with the Wiskott-Aldrich syndrome

✍ Wenda L. Greer; Amro Shehabeldin; Jerry Schulman; Anne Junker; K. A. Siminovitch 📂 Article 📅 1996 🏛 Springer 🌐 English ⚖ 40 KB

Identification of novel and known KRT5 a

Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype

✍ M.J. Arin; G. Grimberg; H. Schumann; H. De Almeida Jr; Y.-R. Chang; G. Tadini; J 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 161 KB

Identification of 29 novel and nine recu

Identification of 29 novel and nine recurrent fibrillin-1 (FBN1) mutations and genotype–phenotype correlations in 76 patients with Marfan syndrome

✍ Kathrin Rommel; Matthias Karck; Axel Haverich; Yskert von Kodolitsch; Meike Rybc 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 180 KB

## Communicated by Jurgen Horst Marfan syndrome (MFS) is an autosomal-dominant disorder of the fibrous connective tissue that is typically caused by mutations in the gene coding for fibrillin-1 (FBN1), a major component of extracellular microfibrils. The clinical spectrum of MFS is highly variable

Identification of 12 novel mutations and

Identification of 12 novel mutations and two new polymorphisms in the arylsulfatase A gene: Haplotype and genotype–phenotype correlation studies in spanish metachromatic leukodystrophy patients

✍ Laura Gort; M. Josep Coll; Amparo Chabás 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 305 KB 👁 2 views

Arylsulfatase A (ARSA) deficiency is the main cause of metachromatic leukodystrophy (MLD), a lysosomal disorder with no specific treatment. In view of the importance of genetic counseling, analyses of mutations and polymorphisms, including the ARSA pseudodeficiency allele, were carried out in 18 unr