Connection

Contact Us
If you have any questions or feedback please contact us.

Search Results to Tamim H Shaikh

This is a "connection" page, showing the details of why an item matched the keywords from your search.

Search Results

Shaikh, Tamim

One or more keywords matched the following items that are connected to Shaikh, Tamim

Item Type	Name
Academic Article	A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects.
Academic Article	Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).
Academic Article	Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint.
Academic Article	Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).
Academic Article	A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.
Academic Article	Detailed analysis of 22q11.2 with a high density MLPA probe set.
Academic Article	A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
Academic Article	Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.
Academic Article	The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.
Academic Article	Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families.
Academic Article	Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review.
Academic Article	Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.
Academic Article	High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor.
Academic Article	Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors.
Concept	Chromosomes, Human, Pair 22
Academic Article	The 22q11 low copy repeats are characterized by unprecedented size and structural variability.

Search Criteria

Chromosomes Human Pair 22