Pages that link to "Q28288492"

The following pages link to The 1993-94 Généthon human genetic linkage map (Q28288492):

Displaying 50 items.

• Initial sequencing and analysis of the human genome (Q21045365) (← links)
• Cloning of the human uroplakin 1B cDNA and analysis of its expression in urothelial-tumor cell lines and bladder-carcinoma tissue (Q22001476) (← links)
• Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes (Q22003988) (← links)
• Interleukin-1 receptor cluster: gene organization of IL1R2, IL1R1, IL1RL2 (IL-1Rrp2), IL1RL1 (T1/ST2), and IL18R1 (IL-1Rrp) on human chromosome 2q (Q22009143) (← links)
• Plakophilin 3--a novel cell-type-specific desmosomal plaque protein (Q22010141) (← links)
• Finishing the euchromatic sequence of the human genome (Q22122488) (← links)
• The pro-alpha3(V) collagen chain. Complete primary structure, expression domains in adult and developing tissues, and comparison to the structures and expression domains of the other types V and XI procollagen chains (Q22253347) (← links)
• Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy (Q24304076) (← links)
• Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure (Q24309024) (← links)
• A human MSX1 homeodomain missense mutation causes selective tooth agenesis (Q24310369) (← links)
• Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias (Q24311437) (← links)
• Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family (Q24311501) (← links)
• A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease (Q24311512) (← links)
• Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter (Q24311551) (← links)
• β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12 (Q24312878) (← links)
• Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2 (Q24313292) (← links)
• The Bloom's syndrome gene product is homologous to RecQ helicases (Q24313440) (← links)
• Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus (Q24313449) (← links)
• Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease (Q24316501) (← links)
• A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome (Q24316980) (← links)
• The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9 (Q24317238) (← links)
• Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III (Q24317311) (← links)
• Mutation of HOXA13 in hand-foot-genital syndrome (Q24318467) (← links)
• Human PEG1/MEST, an imprinted gene on chromosome 7 (Q24322948) (← links)
• MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO) (Q24324139) (← links)
• Isolation and characterization of cDNAs encoding PDE5A, a human cGMP-binding, cGMP-specific 3',5'-cyclic nucleotide phosphodiesterase (Q24336601) (← links)
• A gene for familial venous malformations maps to chromosome 9p in a second large kindred (Q24517883) (← links)
• Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis (Q24517892) (← links)
• Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasia (Q24517904) (← links)
• Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22 (Q24517924) (← links)
• Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene. (Q24517948) (← links)
• Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23 (Q24536215) (← links)
• The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p. (Q24538682) (← links)
• Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34. (Q24538838) (← links)
• Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. (Q24538863) (← links)
• A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3 (Q24539096) (← links)
• A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33. (Q24539175) (← links)
• Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p. (Q24539327) (← links)
• Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia (Q24540027) (← links)
• Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13 (Q24540072) (← links)
• Identification of a new locus for medullary cystic disease, on chromosome 16p12. (Q24540073) (← links)
• Mapping of primary congenital lymphedema to the 5q35.3 region (Q24540112) (← links)
• A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity (Q24540152) (← links)
• Juvenile hemochromatosis locus maps to chromosome 1q. (Q24540265) (← links)
• Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein (Q24561566) (← links)
• Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene (Q24561688) (← links)
• A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity (Q24564608) (← links)
• A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene (Q24597804) (← links)
• 2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4 (Q24603242) (← links)
• Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex (Q24627151) (← links)