Pages that link to "Q35195088"

The following pages link to Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis (Q35195088):

Displaying 30 items.

• Analysis of chromosome 21 yeast artificial chromosome (YAC) clones (Q24679560) (← links)
• Redox proteomics in selected neurodegenerative disorders: from its infancy to future applications. (Q30446460) (← links)
• A contiguous 3-Mb sequence-ready map in the S3-MX region on 21q22.2 based on high- throughput nonisotopic library screenings. (Q30671252) (← links)
• Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection library (Q33232000) (← links)
• Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21 (Q34325983) (← links)
• Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1. (Q34389384) (← links)
• Maternal age effect: The enigma of Down syndrome and other trisomic conditions (Q35148541) (← links)
• Overexpression of esterase D in kidney from trisomy 13 fetuses (Q35194933) (← links)
• A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21. (Q35195145) (← links)
• No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21 (Q35196333) (← links)
• Down syndrome phenotypes: the consequences of chromosomal imbalance (Q35344729) (← links)
• Williams syndrome associated with complete atrioventricular septal defect (Q35581127) (← links)
• Non congenital heart disease aspects of Down's syndrome. (Q35597736) (← links)
• Cytogenetic and molecular studies of Down syndrome individuals with leukemia. (Q35643435) (← links)
• Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18. (Q35889727) (← links)
• Genetic modifiers predisposing to congenital heart disease in the sensitized Down syndrome population (Q36068173) (← links)
• Down Syndrome Related Muscle Hypotonia: Association with COL6A3 Functional SNP rs2270669. (Q36781858) (← links)
• The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies (Q37259226) (← links)
• 4-Hydroxy-2-nonenal, a reactive product of lipid peroxidation, and neurodegenerative diseases: a toxic combination illuminated by redox proteomics studies (Q37960537) (← links)
• Isolation, characterization and genetic analysis of canine GATA4 gene in a family of Doberman Pinschers with an atrial septal defect. (Q38502097) (← links)
• The Role of β-Amyloid in the Development of Alzheimerʼs Disease (Q40425515) (← links)
• Down syndrome and consanguinity (Q41950060) (← links)
• WRB is the receptor for TRC40/Asna1-mediated insertion of tail-anchored proteins into the ER membrane (Q42280602) (← links)
• Methods for genetic linkage analysis using trisomies. (Q42743148) (← links)
• Collagen type VI expression during cardiac development and in human fetuses with trisomy 21 (Q52097890) (← links)
• Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects. (Q55654778) (← links)
• Molecular analysis of the expression of transthyretin in intestine and liver from trisomy 18 fetuses (Q61951268) (← links)
• Never too Grown-Up for a Congenital Heart Disease: Diagnosis of Transitional Atrioventricular Canal in a 50-Year-Old Male (Q64298905) (← links)
• Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21 (Q72253491) (← links)
• Molecular mechanisms of congenital heart disease in down syndrome (Q91940282) (← links)