Negligible interchromosomal effect in embryos of Robertsonian translocation carriers

Reproductive BioMedicine Online

Volumn 10, Issue 3, 2005, Pages 363-369

  Munné, Santiago ^a   Escudero, Tomas ^a   Fischer, Jill ^a,b   Chen, Serena ^b   Hill, Joseph ^c   Stelling, James R ^d   Estop, Anna ^e  

^a Reprogenetics LLC   (United States)

^b Inst Repro Med Sci S B   (United States)

^c Fertility Centers of New England   (United States)

^d Reproductive Specialists of NY   (United States)

^e NONE

Author keywords

Mosaicism; PGD; t(13; 14); t(13; 22); t(14; 15); t(14; 21)

Indexed keywords

ANEUPLOIDY; ARTICLE; CHROMOSOME 16; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME 22; CHROMOSOME ABERRATION; CHROMOSOME PAIRING; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CONTROLLED STUDY; DNA PROBE; EMBRYO DEVELOPMENT; FEMALE; FERTILIZATION IN VITRO; FLUORESCENCE IN SITU HYBRIDIZATION; GAMETE; GENETIC PREDISPOSITION; GENETIC SCREENING; HETEROZYGOTE; HUMAN; INCIDENCE; KARYOTYPE; KARYOTYPE 46,XY; MALE; MONOGENIC DISORDER; MOSAICISM; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDY; RISK ASSESSMENT; ROBERTSONIAN CHROMOSOME TRANSLOCATION; STATISTICAL ANALYSIS; TRISOMY; X CHROMOSOME LINKED DISORDER; ZYGOTE;

EID: 14944366531     PISSN: 14726483     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1472-6483(10)61797-X     Document Type: Article

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