Normal view MARC view ISBD view

[Diversity in the bacterial genus Halomonadaceae in the Upper Kama salts mining region]. [electronic resource]

By:

Korsakova, E S

Contributor(s):

Producer: 20130806Description: 247-50 p. digitalISSN:

0026-3656

Subject(s):

Online resources:

Available from publisher's website

In: Mikrobiologiia vol. 82

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article

There are no comments on this title.

to post a comment.

Back to results

1 X linked mental retardation.
by Rejeb, Imen
2 Allele frequency distribution of the D1S80 VNTR locus in a Tunisian population.
by Kallel, Faouzi
3 Subtelomeric microduplications in three sisters with moderate mental retardation.
by Hila, Lamia
4 Detection of a frequent duplicated CYP21A2 gene carrying a Q318X mutation in a general population with quantitative PCR methods.
by Kharrat, Maher
5 [Interest of studying subtelomeric abnormalities by in situ fluorescent hybridization to explore idiopathic mental retardation].
by Hila, Lamia
6 Autism: an overview of genetic aetiology.
by Bayou, Nadia
7 A novel 13-bp deletion in exon 1 of CYP21 gene causing severe congenital adrenal hyperplasia.
by Kharrat, Maher
8 [Genetics of inflammatory bowel disease].
by Zouiten, Mekki Lilia
9 MLPA subtelomere analysis in Tunisian mentally retarded patients.
by Hila, Lamia
10 Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies: a third case report.
by Chaabouni, Myriam
11 Coexistence of Behçet's disease with ankylosing spondylitis and familial Mediterranean fever: a rare occurrence.
by Frigui, Makram
12 Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation.
by Chograni, Manèl
13 Exploring the 7p22.1 chromosome as a candidate region for autism.
by Bayou, Nadia
14 Pallister-Killian syndrome with additional manifestations of cleft palate and sacral appendage.
by Chaouachi, Sihem
15 [Molecular diagnosis of fragile X syndrome].
by Ben Jemaa, Lamia
16 Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family.
by Chaabouni, Myriam
17 GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
by Trabelsi, Mediha
18 Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation.
by Kharrat, Maher
19 [Treacher-Collins syndrome: clinical and genetic aspects apropos of 4 cases of which 1 is familial].
by Chaabouni, Myriam
20 A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardation.
by Rejeb, Imen