Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  20 results for ""Chromosomes, Human, Pair 11""

Your Filters

Geographic : italy
Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: results from a multicenter study in Italy.

  • Authors : Silvestri V; Department of Molecular Medicine, Sapienza University of Rome, Italy.; Rizzolo P

Subjects: Chromosomes, Human, Pair 11* ; Chromosomes, Human, Pair 14* ; Chromosomes, Human, Pair 8*

  • Source: European journal of cancer (Oxford, England : 1990) [Eur J Cancer] 2015 Nov; Vol. 51 (16), pp. 2289-95. Date of Electronic Publication: 2015 Aug 03.Publisher: Elsevier Science Ltd Country of Publication: England NLM ID: 9005373 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

ATM whole gene deletion in an Italian family with hereditary pancreatic cancer: Challenges to cancer risk prediction associated with an 11q22.3 microdeletion.

  • Authors : Arts HH; McMaster University, Department of Pathology and Molecular Medicine, 1280 Main Street West, L8S 4L8, Hamilton, ON, Canada.; Lynch L

Subjects: Adenocarcinoma/Adenocarcinoma/Adenocarcinoma/*genetics ; Ataxia Telangiectasia Mutated Proteins/Ataxia Telangiectasia Mutated Proteins/Ataxia Telangiectasia Mutated Proteins/*genetics ; Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/*genetics

  • Source: Cancer genetics [Cancer Genet] 2020 Jan; Vol. 240, pp. 1-4. Date of Electronic Publication: 2019 Oct 12.Publisher: Elsevier Country of Publication: United States NLM ID: 101539150 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

A large deletion on chromosome 11 in acute intermittent porphyria.

  • Authors : Di Pierro E; Department of Internal Medicine, Maggiore Policlinico, Mangiagalli and Regina Elena, Foundation IRCCS, University of Milan, Italy.; Besana V

Subjects: Chromosome Deletion* ; Chromosomes, Human, Pair 11*; Porphyria, Acute Intermittent/Porphyria, Acute Intermittent/Porphyria, Acute Intermittent/*genetics

  • Source: Blood cells, molecules & diseases [Blood Cells Mol Dis] 2006 Jul-Aug; Vol. 37 (1), pp. 50-4. Date of Electronic Publication: 2006 Jul 07.Publisher: Academic Press Country of Publication: United States NLM ID: 9509932 Publication Model: Print-Electronic Cited Medium: Print ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Interphase fluorescence in situ hybridization analysis of del(11)(q23) and del(17)(p13) in chronic lymphocytic leukemia. a study of 40 early-onset patients.

  • Authors : Doneda L; Department of Biology and Genetics Medical Faculty, University of Milan, Milan, Italy. ; Montillo M

Subjects: Chromosome Deletion*; Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/*ultrastructure ; Chromosomes, Human, Pair 17/Chromosomes, Human, Pair 17/Chromosomes, Human, Pair 17/*ultrastructure

  • Source: Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jan 01; Vol. 140 (1), pp. 31-6.Publisher: Elsevier/North-Holland Country of Publication: United States NLM ID: 7909240 Publication Model: Print Cited Medium: Print ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemia.

  • Authors : Garte S; UMDNJ-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.; Taioli E

Subjects: Chromosomes, Human, Pair 11* ; Gene Deletion* ; Genetic Predisposition to Disease*

  • Source: Leukemia research [Leuk Res] 2000 Nov; Vol. 24 (11), pp. 971-4.Publisher: Pergamon Press Country of Publication: England NLM ID: 7706787 Publication Model: Print Cited Medium: Print ISSN: 0145-2126 (Print)

Record details

Read More Add to Saved list
×
Academic Journal

Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).

Subjects: Chromosomes, Human, Pair 11*; Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/Charcot-Marie-Tooth Disease/*genetics ; Myelin Sheath/Myelin Sheath/Myelin Sheath/*pathology

  • Source: Annals of the New York Academy of Sciences [Ann N Y Acad Sci] 1999 Sep 14; Vol. 883, pp. 47-55.Publisher: New York Academy of Sciences Country of Publication: United States NLM ID: 7506858 Publication Model: Print Cited Medium: Print ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Structure and mutation analysis of the glycogen storage disease type 1b gene.

Subjects: Chromosomes, Human, Pair 11* ; Mutation*; Glycogen Storage Disease Type I/Glycogen Storage Disease Type I/Glycogen Storage Disease Type I/*genetics

  • Source: FEBS letters [FEBS Lett] 1998 Oct 02; Vol. 436 (2), pp. 247-50.Publisher: John Wiley & Sons Ltd Country of Publication: England NLM ID: 0155157 Publication Model: Print Cited Medium: Print ISSN: 0014-5793

Record details

Read More Add to Saved list
×
Academic Journal

Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia.

  • Authors : Colombi M; Department of Biomedical Sciences and Biotechnology, University of Brescia, Italy.; Gardella R

Subjects: Chromosomes, Human, Pair 11*; Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*genetics ; Epidermolysis Bullosa Dystrophica/Epidermolysis Bullosa Dystrophica/Epidermolysis Bullosa Dystrophica/*genetics

  • Source: Human genetics [Hum Genet] 1992 Jul; Vol. 89 (5), pp. 503-7.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print Cited Medium: Print ISSN: 0340-6717 (Print)

Record details

Read More Add to Saved list
×
Academic Journal

Short arm of chromosome 11 and sporadic Alzheimer's disease: catalase and cathepsin D gene polymorphisms.

  • Authors : Capurso C; Department of Geriatrics, University of Foggia, Ospedali Riuniti, Viale L. Pinto, 71100 Foggia, Italy. ; Solfrizzi V

Subjects: Polymorphism, Genetic*; Alzheimer Disease/Alzheimer Disease/Alzheimer Disease/*genetics ; Catalase/Catalase/Catalase/*genetics

  • Source: Neuroscience letters [Neurosci Lett] 2008 Feb 27; Vol. 432 (3), pp. 237-42. Date of Electronic Publication: 2007 Dec 23.Publisher: Elsevier Scientific Publishers Ireland Country of Publication: Ireland NLM ID: 7600130 Publication Model: Print-Electronic Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1.

Subjects: Chromosome Mapping*; Candidiasis, Chronic Mucocutaneous/Candidiasis, Chronic Mucocutaneous/Candidiasis, Chronic Mucocutaneous/*genetics ; Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/*genetics

  • Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2003 Jun; Vol. 11 (6), pp. 433-6.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Print ISSN: 1018-4813

Record details

Read Online Read More Add to Saved list
×
  • 1-10 of  20 results for ""Chromosomes, Human, Pair 11""