Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice

Prenatal Diagnosis

Volumn 35, Issue 10, 2015, Pages 1022-1029

  Westerfield, Lauren E ^a   Stover, Samantha R ^a   Mathur, Veena S ^a   Nassef, Salma A ^a   Carter, Tiffiney G ^a   Yang, Yaping ^a,b   Eng, Christine M ^a,b   Van den Veyver, Ignatia B ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b BAYLOR GENETICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; CLINICAL GENETICS; CLINICAL PRACTICE; CONCEPTION; CONGENITAL MALFORMATION; CONTROLLED STUDY; COORDINATION; DIAGNOSTIC TEST; EXOME; FAMILY ASSESSMENT; FAMILY HISTORY; FEMALE; FETUS MALFORMATION; GENE IDENTIFICATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC COUNSELING; HEALTH CARE COST; HEALTH INSURANCE; HUMAN; MEDICAL RECORD REVIEW; MOLECULAR DIAGNOSIS; PATIENT COUNSELING; PATIENT REFERRAL; PERSONAL EXPERIENCE; PREGNANCY; PRENATAL CARE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PRIVATE PRACTICE; REPRODUCTION; RETROSPECTIVE STUDY; TREATMENT INDICATION; TURNAROUND TIME; WHOLE EXOME SEQUENCE; DNA SEQUENCE; PROCEDURES;

EXOME; FEMALE; GENETIC COUNSELING; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDIES; SEQUENCE ANALYSIS, DNA;

EID: 84943262415     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.4674     Document Type: Article

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