Molecular and cytogenetic analysis of familial Xp deletions

American Journal of Medical Genetics

Volumn 94, Issue 2, 2000, Pages 163-169

  Wandstrat, Amy E ^a   Conroy, Jeffrey M ^a   Zurcher, Vickie L ^a   Pasztor, Linda M ^b   Clark, Brian A ^c   Zackowski, Joleen L ^d   Schwartz, Stuart ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CHILDREN S MERCY HOSPITAL   (United States)

^c LERNER RESEARCH INSTITUTE   (United States)

^d EASTERN VIRGINIA MEDICAL SCHOOL   (United States)

Author keywords

Deletion; FISH; Short stature; X chromosome

Indexed keywords

DNA;

ADULT; ARTICLE; CHROMOSOME DELETION X; CHROMOSOME MAP; CHROMOSOME REARRANGEMENT; CHROMOSOME XP; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; FAMILIAL DISEASE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HUMAN; HUMAN CELL; MOLECULAR GENETICS; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCHOOL CHILD; SHORT STATURE; X CHROMOSOME INACTIVATION;

BODY HEIGHT; CHROMOSOME BANDING; CHROMOSOME DELETION; CYTOGENETIC ANALYSIS; DOSAGE COMPENSATION, GENETIC; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; X CHROMOSOME;

EID: 0033844320     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20000911)94:2<163::AID-AJMG9>3.0.CO;2-U     Document Type: Article

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