Pages that link to "Q33874077"
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The following pages link to Systematic cloning of human minisatellites from ordered array charomid libraries. (Q33874077):
Displaying 50 items.
- Comparative genomics and molecular dynamics of DNA repeats in eukaryotes (Q24650948) (← links)
- Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms (Q24676539) (← links)
- Increased rate of spontaneous mitotic recombination in T lymphocytes from a Bloom's syndrome patient using a flow-cytometric assay at HLA-A locus (Q28246783) (← links)
- Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development (Q28282578) (← links)
- Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene (Q28775974) (← links)
- Loss of constitutional heterozygosity on chromosome 5q in hepatocellular carcinoma without cirrhosis (Q30486880) (← links)
- Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors (Q30541671) (← links)
- Multilocus DNA fingerprints in gallinaceous birds: general approach and problems (Q31002084) (← links)
- Recent advances in minisatellite biology (Q33230826) (← links)
- Uniparental paternal disomy in Angelman's syndrome (Q33244469) (← links)
- Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome (Q33595781) (← links)
- Molecular mechanisms in Angelman syndrome: a survey of 93 patients (Q33595952) (← links)
- Measurement of locus copy number by hybridisation with amplifiable probes (Q33612453) (← links)
- Study on possible increase in twinning rate at a small village in south Brazil (Q34428578) (← links)
- Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups (Q34614818) (← links)
- The incidence of mini- and micro-satellite repetitive DNA in the canine genome (Q35029933) (← links)
- Molecular studies of trisomy 18 (Q35194706) (← links)
- Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy (Q35195992) (← links)
- Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients (Q35204517) (← links)
- Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation. (Q35239185) (← links)
- The evolution of molecular markers--just a matter of fashion? (Q35604225) (← links)
- Position effect of human telomeric repeats on replication timing (Q35650825) (← links)
- Genetic evidence that placental site trophoblastic tumours can originate from a hydatidiform mole or a normal conceptus (Q35993578) (← links)
- Charomid cloning vectors meet the pedipalpal chelae: single-locus minisatellite DNA probes for paternity assignment in the harlequin beetle-riding pseudoscorpion (Q36725950) (← links)
- Characterization of tomato DNA clones with sequence similarity to human minisatellites 33.6 and 33.15. (Q36753463) (← links)
- A panel of VNTR markers in pigs (Q36802789) (← links)
- Oligonucleotide Fingerprinting Using Simple Repeat Motifs: A Convenient, Ubiquitously Applicable Method to Detect Hypervariability for Multiple Purposes (Q37098749) (← links)
- The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation (Q38509518) (← links)
- STS for minisatellite MS607 (D22S163). (Q40504423) (← links)
- A highly polymorphic minisatellite (pMS627) on chromosome 14 (D14S44). (Q40507692) (← links)
- A highly polymorphic minisatellite (pMS626) on chromosome 13 (D13S103). (Q40507705) (← links)
- A polymorphic minisatellite (pMS628) on chromosome 3 (D3S1084) (Q40507712) (← links)
- A hypervariable minisatellite (pMS400) on chromosome 19 (D19S176). (Q40508821) (← links)
- A hypervariable minisatellite (pMS502) on chromosome 8 (D8S162). (Q40508827) (← links)
- The proterminal regions and telomeres of human chromosomes. (Q40519621) (← links)
- The efficiency of multilocus DNA fingerprint probes for individualization and establishment of family relationships, determined from extensive casework (Q40561735) (← links)
- The pseudoautosomal regions of the human sex chromosomes (Q40774097) (← links)
- Mutation processes at human minisatellites. (Q40959180) (← links)
- DNA diagnosis of human genetic individuality (Q41073241) (← links)
- Distinct 15q genotypes in Russell-Silver and ring 15 syndromes (Q41221060) (← links)
- Cytogenetic and molecular analysis of 6q deletions in Burkitt's lymphoma cell lines (Q41507372) (← links)
- Loss of constitutional heterozygosity on chromosomes 5 and 17 in cholangiocarcinoma (Q42263314) (← links)
- Loss of heterozygosity on chromosomes 1 and 11 in carcinoma of the pancreas (Q42371964) (← links)
- Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q. (Q42658122) (← links)
- Frequent rearrangements at minisatellite loci D1S7 (1p33-35), D7S22 (7q36-ter) and D12S11 (12q24.3-ter) in hepatitis B virus-positive hepatocellular carcinomas from Thai patients (Q45761885) (← links)
- Highly polymorphic microsatellites in the house sparrow Passer domesticus (Q48065286) (← links)
- Distribution of tandem repeat polymorphism within minisatellite MS621 (D5S110). (Q48067400) (← links)
- Polymorphic microsatellite DNA markers in the grey red-backed vole Clethrionomys rufocanus bedfordiae. (Q48075291) (← links)
- Human minisatellite alleles detectable only after PCR amplification (Q48190170) (← links)
- Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome (Q48427339) (← links)