Pages that link to "Q39819290"

The following pages link to Cytogenetics of pregnancy wastage (Q39819290):

Displaying 34 items.

• Preimplantation genetic diagnosis in clinical practice (Q24679846) (← links)
• Epidemiologic tools to study the influence of environmental factors on fecundity and pregnancy-related outcomes (Q26829247) (← links)
• Highly conserved repetitive DNA sequences are present at human centromeres (Q31116318) (← links)
• Phenotypic expression of the first liveborn 68,XX triploid newborn (Q33597954) (← links)
• New tools for embryo selection: comprehensive chromosome screening by array comparative genomic hybridization (Q33616513) (← links)
• Extreme methylation values of imprinted genes in human abortions and stillbirths (Q33703623) (← links)
• Correlation between missed abortion and insertional translocation involving chromosomes 1 and 7 (Q34176385) (← links)
• Female meiosis drives karyotypic evolution in mammals (Q34613738) (← links)
• Maternal age effect: The enigma of Down syndrome and other trisomic conditions (Q35148541) (← links)
• Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion (Q35195591) (← links)
• Implantation in Patients Over 40 and Raising FSH Levels—a Review (Q35559578) (← links)
• Aneusomy detection with Karyolite-Bac on Beads® is a cost-efficient and high throughput strategy in the molecular analyses of the early pregnancy conception losses (Q35945917) (← links)
• The cytogenetics of preimplantation human development: insights provided by traditional and novel techniques (Q36092891) (← links)
• In vivo binding of active heat shock transcription factor 1 to human chromosome 9 heterochromatin during stress. (Q36324150) (← links)
• What about superfertility, decidualization, and natural selection? (Q36910167) (← links)
• Canine and feline pregnancy loss due to viral and non-infectious causes: a review (Q37189183) (← links)
• A comparative cytogenetic study of miscarriages after IVF and natural conception in women aged under and over 35 years. (Q37601074) (← links)
• Use of cross-species in-situ hybridization (ZOO-FISH) to assess chromosome abnormalities in day-6 in-vivo- or in-vitro-produced sheep embryos (Q38462983) (← links)
• The cumulative dose of gonadotropins used for controlled ovarian stimulation does not influence the odds of embryonic aneuploidy in patients with normal ovarian response (Q38892052) (← links)
• Gene-rich chromosome regions and autosomal trisomy. A case of chromosome 3 trisomy mosaicism (Q39679264) (← links)
• The heteromorphic marker on chromosome 18 using restriction endonuclease AluI. (Q40617032) (← links)
• Maternal Anti‐Placental Cell‐Mediated Reactivity and Spontaneous Abortions (Q41535737) (← links)
• Aneuploidy involving chromosome 1 in failed-fertilized human oocytes is unrelated to maternal age. (Q46032152) (← links)
• Differentiation of genetic abnormalities in early pregnancy loss. (Q50625958) (← links)
• Description of cytogenetic abnormalities and the pregnancy outcomes of couples with recurrent pregnancy loss in a tertiary-care center in Saudi Arabia (Q52354553) (← links)
• The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortions. (Q53038190) (← links)
• Androgenetic origin of African complete hydatidiform moles demonstrated by HLA markers. (Q53905071) (← links)
• Surface and branching of placental villi in early abortion: relationship to karyotype. Scanning electron microscopic study (Q68341230) (← links)
• Significance of structural chromosome aberrations in human sperm: analysis of induced aberrations (Q68583853) (← links)
• A cytogenetic study directly from chorionic villi of 140 spontaneous abortions (Q69398555) (← links)
• Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions? (Q69638927) (← links)
• Triple trisomy in a 17-week-old fetus (Q70221923) (← links)
• Flow cytometric and cytogenetic analyses in human spontaneous abortions (Q72788459) (← links)
• Association between hereditary predisposition to common cancers and congenital multimalformations (Q91746043) (← links)