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Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium
MOLECULAR PSYCHIATRY
Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15
EUROPEAN JOURNAL OF HUMAN GENETICS
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A
HUMAN MOLECULAR GENETICS
Comparative mapping of BTA15 and HSA11 including a region containing a QTLfor meat tenderness
MAMMALIAN GENOME
Construction of a high-resolution RH map of the human 2q35 region on TNG panel and comparison with a physical map of the porcine homologous region 15q25
MAMMALIAN GENOME
Behavioral phenotypes of genetic syndromes: A reference guide for psychiatrists
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
Circletail, a new mouse mutant with severe neural tube defects: Chromosomal localization and interaction with the loop-tail mutation
GENOMICS
Comparative analysis of a BAC contig of the porcine RN region and the human transcript map: Implications for the cloning of trait loci
GENOMICS
Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24
GENOMICS
Genome scans for susceptibility genes in bipolar affective disorder
ANNALS OF MEDICINE
Thromboendarterectomy of the right common iliac artery in a patient with Marfan's syndrome and restoration with a new technique
INTERNATIONAL ANGIOLOGY
Polyploidy in acute promyelocytic leukemia without the 15 : 17 translocation
HAEMATOLOGICA
Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 butnot intron 7
HUMAN GENETICS
Association study of a nicotinic receptor variant with schizophrenic disorders
NEUROPSYCHOBIOLOGY
Linkage mapping of MMP1 to cattle chromosome 15
ANIMAL GENETICS
Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development
PRENATAL DIAGNOSIS
The effect of nicotine and haloperidol co-treatment on nicotinic receptor levels in the rat brain
MOLECULAR BRAIN RESEARCH
GABA(A) receptor beta 3 subunit gene and psychiatric morbidity in a post-traumatic stress disorder population
PSYCHIATRY RESEARCH
Characterization of microsatellite markers flanking FBN1: Utility in the diagnostic evaluation for Marfan syndrome
AMERICAN JOURNAL OF MEDICAL GENETICS
Rearrangements of chromosome 15 in epilepsy
AMERICAN JOURNAL OF MEDICAL GENETICS
Examination of genetic linkage of chromosome 15 to schizophrenia in a large veterans affairs cooperative study sample
AMERICAN JOURNAL OF MEDICAL GENETICS
Evidence for linkage disequilibrium between the alpha 7-nicotinic receptorgene (CHRNA7) locus and schizophrenia in Azorean families
AMERICAN JOURNAL OF MEDICAL GENETICS
The phenotypic manifestations of interstitial duplications of proximal 15qwith special reference to the autistic spectrum disorders
AMERICAN JOURNAL OF MEDICAL GENETICS
Evidence for the multigenic inheritance of schizophrenia
AMERICAN JOURNAL OF MEDICAL GENETICS
GABA-A receptor beta 3 and alpha 5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: A genetic association study
AMERICAN JOURNAL OF MEDICAL GENETICS
Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the alpha 7-nicotinic acetylcholine receptor subunit gene (CHRNA7)
AMERICAN JOURNAL OF MEDICAL GENETICS
Duplication of 15q11.2-q14, including the P gene, in a woman with generalized skin hyperpigmentation
AMERICAN JOURNAL OF MEDICAL GENETICS
Congenital glaucoma and silver-russell phenotype associated with partial trisomy 7q and monosomy 15q
AMERICAN JOURNAL OF MEDICAL GENETICS
Minute supernumerary marker chromosomes identified in two patients with a related, larger pseudodicentric chromosome
AMERICAN JOURNAL OF MEDICAL GENETICS
Methylation, cytogenetic and FISH tests in the molecular diagnosis of Prader-Willi and Angelman syndromes
REVISTA MEDICA DE CHILE
The changing purpose of Prader-Willi syndrome clinical diagnostic criteriaand proposed revised criteria
PEDIATRICS
De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes
JOURNAL OF MEDICAL GENETICS
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14
JOURNAL OF MEDICAL GENETICS
Cutting edge: A/WySnJ transitional B cells overexpress the chromosome 15 proapoptotic Blk gene and succumb to premature apoptosis
JOURNAL OF IMMUNOLOGY
The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome
CLINICAL GENETICS
Upper respiratory tract carcinoma with chromosomal translocation 15;19 - Evidence for a distinct disease entity of young patients with a rapidly fatal course
CANCER
Cigarette smoking and psychotic symptoms in bipolar affective disorder
BRITISH JOURNAL OF PSYCHIATRY
Natural history of cardiovascular manifestations in Marfan syndrome
ARCHIVES OF DISEASE IN CHILDHOOD
The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression
AMERICAN JOURNAL OF HUMAN GENETICS
Disruption of the bipartite imprinting center in a family with Angelman syndrome
AMERICAN JOURNAL OF HUMAN GENETICS
Gene expression in hypothalamus and brown adipose tissue of mice divergently selected for heat loss
PHYSIOLOGICAL GENOMICS
Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human
GENOME RESEARCH
Maintaining imprinting
NATURE GENETICS
Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
Severe tortuosity and stenosis of the systemic, pulmonary and coronary vessels in 12 patients with similar phenotypic features: a new syndrome?
CARDIOLOGY IN THE YOUNG
A sequence-ready map for human chromosome 12q15-21
DNA SEQUENCE
A high-density linkage map of the RN region in pigs
GENETICS SELECTION EVOLUTION
The genetics of schizophrenia
CURRENT OPINION IN PSYCHIATRY
The chronic proliferative dermatitis mouse mutation (cpdm): mapping of themutant gene locus
JOURNAL OF EXPERIMENTAL ANIMAL SCIENCE
Mapping of obesity QTLs in a cross between mouse lines divergently selected on fat content
MAMMALIAN GENOME
The alpha 7-nicotinic acetylcholine receptor and the pathology of hippocampal interneurons in schizophrenia
JOURNAL OF CHEMICAL NEUROANATOMY
Ocat, a paternally expressed gene closely linked and transcribed in the opposite direction to Peg3
GENOMICS
Testing for the RN- gene in retail pork chops
MEAT SCIENCE
Retrospective diagnosis of trisomy 15 in formalin-fixed, paraffin-embeddedplacental tissue in a newborn girl with Prader-Willi syndrome
PRENATAL DIAGNOSIS
Inhibitory neurophysiological deficit as a phenotype for genetic investigation of schizophrenia
AMERICAN JOURNAL OF MEDICAL GENETICS
Search for bipolar disorder susceptibility loci: The application of a modified genome scan concentrating on gene-rich regions
AMERICAN JOURNAL OF MEDICAL GENETICS
Schizophrenia and smoking: Evidence for a common neurobiological basis?
AMERICAN JOURNAL OF MEDICAL GENETICS
Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families
AMERICAN JOURNAL OF MEDICAL GENETICS
No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
AMERICAN JOURNAL OF MEDICAL GENETICS
Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation
AMERICAN JOURNAL OF MEDICAL GENETICS
Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome
AMERICAN JOURNAL OF MEDICAL GENETICS
Tetrasomy 15q25 -> qter: Cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome
AMERICAN JOURNAL OF MEDICAL GENETICS
Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15
AMERICAN JOURNAL OF MEDICAL GENETICS
Paternal UPD15: Further genetic and clinical studies in four Angelman syndrome patients
AMERICAN JOURNAL OF MEDICAL GENETICS
Two novel fibrillin-2 mutations in congenital contractural arachnodactyly
AMERICAN JOURNAL OF MEDICAL GENETICS
Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: Effects of imprinting
AMERICAN JOURNAL OF MEDICAL GENETICS
A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle
SCIENCE
Molecular genetic diagnosis of Prader-Willi and Angelman syndrome using a methylation-specific polymerase chain reaction
MONATSSCHRIFT KINDERHEILKUNDE
Two translocations of chromosome 15q associated with dyslexia
JOURNAL OF MEDICAL GENETICS
Frequency of the rendement napole RN- allele in a population of American Hampshire pigs
JOURNAL OF ANIMAL SCIENCE
Smoking and schizophrenia: abnormal nicotinic receptor expression
EUROPEAN JOURNAL OF PHARMACOLOGY
Segregation of a supernumerary del(15) marker chromosome in sperm
CLINICAL GENETICS
Familial Prader-Willi syndrome: Case report and a literature review
CLINICAL GENETICS
A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction
CLINICAL GENETICS
The oocyte-specific methylated region of the U2afbp-rs/U2af1-rs1 gene is dispensable for its imprinted methylation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Prolongation of brainstem auditory-evoked responses in autistic probands and their unaffected relatives
ARCHIVES OF GENERAL PSYCHIATRY
Multipoint genetic mapping with uniparental disomy data
AMERICAN JOURNAL OF HUMAN GENETICS
Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome
AMERICAN JOURNAL OF HUMAN GENETICS
Autosome search for schizophrenia susceptibility genes in multiply affected families
MOLECULAR PSYCHIATRY
Familial evans syndrome: A report of an affected sibship
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
The diagnosis of Prader-Willi syndrome
JOURNAL OF PAEDIATRICS AND CHILD HEALTH
A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia)
EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15
EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect
EUROPEAN JOURNAL OF HUMAN GENETICS
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelmansyndrome patients
EUROPEAN JOURNAL OF HUMAN GENETICS
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion
HUMAN MOLECULAR GENETICS
A de novo deletion of chromosome 15(q15.2q21.2) in a dysmorphic, mentally retarded child with congenital scalp defect
CLINICAL DYSMORPHOLOGY
The human CILP gene: exon/intron organization and chromosomal mapping
MATRIX BIOLOGY
Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human
MAMMALIAN GENOME
A radiation hybrid map of the RN region in pigs demonstrates conserved gene order compared with the human and mouse genomes
MAMMALIAN GENOME
Detecting genes in new and old mouse models for epilepsy: a prospectus through the magnifying glass
EPILEPSY RESEARCH
Distinctive pattern of behavioral functioning in Angelman syndrome
AMERICAN JOURNAL ON MENTAL RETARDATION
Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy
AMERICAN JOURNAL ON MENTAL RETARDATION
Clinical, pathological and molecular genetic findings in a case of neonatal Marfan syndrome
ACTA PAEDIATRICA
Cryptic insertion (15;17) in a case of acute promyelocytic leukemia detected by fluorescence in situ hybridization
HAEMATOLOGICA
Diagnosis of Angelman syndrome: clinical and EEG criteria
BRAIN & DEVELOPMENT
Angelman syndrome: a review of clinical and genetic aspects
CLINICAL NEUROLOGY AND NEUROSURGERY
Cloning, sequencing and mapping the pig gene for the muscle-specific intermediate filament protein desmin (DES)
ANIMAL GENETICS
Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion ofuniparental disomy for chromosome 15
PRENATAL DIAGNOSIS
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism
AMERICAN JOURNAL OF MEDICAL GENETICS