The second case of a t[17;22) in a family with neurofibromatosis type 1: Sequence analysis of the breakpoint regions

Human Genetics

Volumn 99, Issue 2, 1997, Pages 237-247

  Kehrer Sawatzki, Hildegard ^a   Haussler, Jürgen ^a   Krone, Winfrid ^a   Bode, Harald ^b   Jenne, Dieter E ^c   Mehnert, Karl U ^d   Tümmers, Ulrich ^e   Assum, Günter ^a  

^a Abteilung Humangenetik   (Germany)

^b Sozialpadiatrisches Zentrum   (Germany)

^c MAX PLANCK INSTITUTE OF PSYCHIATRY   (Germany)

^d Medizinische Genetik   (Germany)

^e NONE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; PRIMER DNA; REPETITIVE DNA;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 13; CHROMOSOME 17Q; CHROMOSOME 22Q; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; COSMID; DNA LIBRARY; DNA SEQUENCE; FEMALE; GENE DISRUPTION; HUMAN; HUMAN CELL; MOLECULAR CLONING; NEUROFIBROMATOSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOUTHERN BLOTTING;

ADULT; BASE SEQUENCE; CELLS, CULTURED; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 22; DNA; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MOLECULAR SEQUENCE DATA; NEUROFIBROMATOSIS 1; RESTRICTION MAPPING; SEQUENCE ALIGNMENT; TRANSLOCATION, GENETIC;

EID: 0031025934     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050346     Document Type: Article

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