Birth of a healthy infant following preimplantation PKHD1 haplotyping for autosomal recessive polycystic kidney disease using multiple displacement amplification

Journal of Assisted Reproduction and Genetics

Volumn 27, Issue 7, 2010, Pages 397-407

  Lau, Eduardo C ^a,b   Janson, Marleen M ^a,b   Roesler, Mark R ^c   Avner, Ellis D ^a,b   Strawn, Estil Y ^a,c   Bick, David P ^a,b  

^a MEDICAL COLLEGE OF WISCONSIN   (United States)

^b Health System of Wisconsin ^*  (United States)

^c FROEDTERT MEMORIAL LUTHERAN HOSPITAL   (United States)

Author keywords

Autosomal recessive polycystic kidney disease; Linkage analysis with linked STR markers; Multiple displacement amplification; PKHD1 haplotype analysis; Preimplantation genetic diagnosis

Indexed keywords

ADULT; ARTICLE; BLASTOMERE; CASE REPORT; CHILDBIRTH; CONTROLLED STUDY; EMBRYO; FEMALE; FERTILIZATION IN VITRO; GENE; GENE AMPLIFICATION; GENE SEQUENCE; GENETIC LINKAGE; GENETIC SCREENING; GENOME; HAPLOTYPE; HUMAN; KIDNEY POLYCYSTIC DISEASE; MARKER GENE; MUTANT; PKHD1 GENE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RELIABILITY; SHORT TANDEM REPEAT;

FEMALE; GENETIC MARKERS; HAPLOTYPES; HUMANS; INFANT; MICROSATELLITE REPEATS; POLYCYSTIC KIDNEY, AUTOSOMAL RECESSIVE; POLYMERASE CHAIN REACTION; PREGNANCY; PREIMPLANTATION DIAGNOSIS; RECEPTORS, CELL SURFACE;

EID: 77956413044     PISSN: 10580468     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10815-010-9432-5     Document Type: Article

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