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AMERICAN JOURNAL OF MEDICAL GENETICS
Rivista
Codice:
E007659
ISSN:
0148-7299
Dati Generali
Dati Generali
Pubblicazioni (22)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A genome-wide scan in 301 families with sibling-pairs diagnosed with schizophrenia of schizoaffective disorder suggests linkage to chromosomes 2pcen and 10p14.
Articolo
A genome-wide search for schizophrenia susceptibility genes.
Articolo
A novel INSL3 mutation associated with human cryptorchidism
Articolo
Additional Support for Schizophrenia Linkage on Chromosomes 6 and 8: A Multicenter Study
Articolo
Cerebro-reno-digital syndrome in two sibs.
Articolo
Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosome
Articolo
Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder.
Articolo
Lack of evidence for linkage to chromosomes 13 and 8 for schizophrenia and schizoaffective disorder
Articolo
Linkage analysis of schizophrenic to chromosome 6p24-p22: an attempt to replicate.
Articolo
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome.
Articolo
Male siblings with schizophrenia share alleles at the androgen receptor above chance expectation.
Articolo
Mild phenotype associated with inv dup 8 (q21.2-q22.3) of maternal origin.
Articolo
Novel X-linked mental retardation syndrome with short stature maps to Xq24.
Articolo
Novel insulin-like 3 (INSL3) gene mutation associated with human cryptorchidism
Articolo
Novel insulin-like 3 (INSL3) gene mutation associated with human cryptorchidism
Articolo
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats.
Articolo
Response to local dihydrotestosterone treatment in a patient with partial androgen-insensitivity syndrome due to a novel mutation in the androgen receptor gene
Articolo
Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structure.
Articolo
Significant evidence for a schizophrenia susceptibility locus in the centromeric region of human chromosome
Articolo
TWO NEW MISSENSE MUTATIONS (A105T AND C110G)IN THE NORRIN GENEIN TWO ITALIAN FAMILIES WITH NORRIE DISEASE AND FAMILIAL EXUDATIVE VITREORETINOPATHY.
Articolo
TWO PEDIGREES OF AUTOSOMAL DOMINANT ATRIOVENTRICULAR CANAL DEFECT (AVCD): EXCLUSION FROM THE CRITICAL REGION ON 8p.
Articolo
X-linked mental retardation with Marfanoid habitus. First report of four italian patients.
Articolo
No Results Found
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