Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22).

scientific article published on July 1999

Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22). is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1093/MOLEHR/5.7.682
P698PubMed publication ID10381825
P5875ResearchGate publication ID277503748

P50authorVan Steirteghem AQ94659758
P2093author name stringLiebaers I
Vandervorst M
Bonduelle M
Staessen C
Van Assche E
Vegetti W
P4510describes a project that usesfluorescence in situ hybridizationQ1336182
P433issue7
P304page(s)682-690
P577publication date1999-07-01
P1433published inMolecular Human ReproductionQ15761794
P1476titlePreimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22).
P478volume5

Reverse relations

cites work (P2860)
Q33608623A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer
Q44412800Blastomere fixation techniques and risk of misdiagnosis for preimplantation genetic diagnosis of aneuploidy
Q53633348Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers.
Q34430699Chromosome segregation analysis in human embryos obtained from couples involving male carriers of reciprocal or Robertsonian translocation
Q79943701Dilemmas encountered with preimplantation diagnosis of aneuploidy in human embryos
Q38495498Effect of chromosomal translocations on the development of preimplantation human embryos in vitro
Q79108677Fluorescence in situ hybridisation (FISH) analysis of chromosome segregation and interchromosomal effect in spermatozoa of a reciprocal translocation t(9,10)(q11;p11.1) carrier
Q34707274Is intracytoplasmic sperm injection safe? Current status and future concerns
Q36271546Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis
Q34162210Meiotic outcomes in reciprocal translocation carriers ascertained in 3-day human embryos
Q37516220Meiotic pairing and gene expression disturbance in germ cells from an infertile boar with a balanced reciprocal autosome-autosome translocation.
Q35843964Meiotic segregation of translocations during male gametogenesis
Q30899679Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.
Q81631790Negligible interchromosomal effect in embryos of Robertsonian translocation carriers
Q90219242Non-invasive prenatal screening for Emanuel syndrome
Q33944569Outcome of preimplantation genetic diagnosis of translocations
Q81318823Predictability of preimplantation genetic diagnosis of aneuploidy and translocations on prospective attempts
Q52014499Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations.
Q81318818Preferential alternate segregation in the common t(11;22)(q23;q11) reciprocal translocation: sperm FISH analysis in two brothers
Q80093090Preimplantation genetic diagnosis
Q73648569Preimplantation genetic diagnosis for sickle-cell anemia and for beta-thalassemia
Q74457872Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders
Q35019247Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities
Q57779363Preimplantation genetic diagnosis of pericentric inversions
Q61842172Preimplantation genetic diagnosis significantly improves the pregnancy outcome of translocation carriers with a history of recurrent miscarriage and unsuccessful pregnancies
Q37995487Prenatal screening characteristics in Emanuel syndrome: a case series and review of the literature.
Q33830561Recent advances and future developments in PGD.
Q53451950Reciprocal translocations: tracing their meiotic behavior.
Q37866921Reproductive outcome after PGD in couples with recurrent miscarriage carrying a structural chromosome abnormality: a systematic review
Q34395407Successful pregnancy outcomes after preimplantation genetic diagnosis (PGD) for carriers of chromosome translocations
Q74592036Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males

Search more.