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11 in total

1. Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers.

Authors: P R Winship; D J Rees; M Alkan
Journal: Lancet Date: 1989-03-25 Impact factor: 79.321

2. Recombination at the human alpha-globin gene cluster: sequence features and topological constraints.

Authors: R D Nicholls; N Fischel-Ghodsian; D R Higgs
Journal: Cell Date: 1987-05-08 Impact factor: 41.582

3. Nucleotide sequence of the gene for human factor IX (antihemophilic factor B).

Authors: S Yoshitake; B G Schach; D C Foster; E W Davie; K Kurachi
Journal: Biochemistry Date: 1985-07-02 Impact factor: 3.162

4. Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

Authors: G Camerino; K H Grzeschik; M Jaye; H De La Salle; P Tolstoshev; J P Lecocq; R Heilig; J L Mandel
Journal: Proc Natl Acad Sci U S A Date: 1984-01 Impact factor: 11.205

5. Segments containing alternating purine and pyrimidine dinucleotides: patterns of polymorphism in humans and prevalence throughout phylogeny.

Authors: G Sarkar; C Paynton; S S Sommer
Journal: Nucleic Acids Res Date: 1991-02-11 Impact factor: 16.971

6. The rates and patterns of deletions in the human factor IX gene.

Authors: R P Ketterling; E L Vielhaber; T J Lind; E C Thorland; S S Sommer
Journal: Am J Hum Genet Date: 1994-02 Impact factor: 11.025

7. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.

Authors: M Koenig; E P Hoffman; C J Bertelson; A P Monaco; C Feener; L M Kunkel
Journal: Cell Date: 1987-07-31 Impact factor: 41.582

8. Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels.

Authors: A Ballabio; R Carrozzo; G Parenti; A Gil; M Zollo; M G Persico; E Gillard; N Affara; J Yates; M A Ferguson-Smith
Journal: Genomics Date: 1989-01 Impact factor: 5.736

9. "Cryptic" repeating triplets of purines and pyrimidines (cRRY(i)) are frequent and polymorphic: analysis of coding cRRY(i) in the proopiomelanocortin (POMC) and TATA-binding protein (TBP) genes.

Authors: B Gostout; Q Liu; S S Sommer
Journal: Am J Hum Genet Date: 1993-06 Impact factor: 11.025

10. Characterization of a large deletion associated with a polymorphic block of repeated dinucleotides in the type III procollagen gene (COL3A1) of a patient with Ehlers-Danlos syndrome type IV.

Authors: B Lee; M D'Alessio; H Vissing; F Ramirez; B Steinmann; A Superti-Furga
Journal: Am J Hum Genet Date: 1991-03 Impact factor: 11.025