Deletion mapping by FISH with BACs in patients with partial monosomy 22q13

Human Genetics

Volumn 102, Issue 5, 1998, Pages 557-561

  Schröder, Kristina ^a   Schuffenhauer, Simone ^b   Seidel, Heide ^b   Bartsch, Oliver ^c   Blin, Nikolaus ^a   Hinkel, Georg Klaus ^c   Schmitt, Holger ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

^c UNIVERSITY HOSPITAL CARL GUSTAV CARUS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MAPPING; GROWTH DISORDER; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; MARKER GENE; MOLECULAR GENETICS; MUSCLE HYPOTONIA; PARTIAL MONOSOMY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT;

CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CLONING, MOLECULAR; DEVELOPMENTAL DISABILITIES; FACE; FEMALE; GROWTH DISORDERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MICROSATELLITE REPEATS; MUSCLE HYPOTONIA;

EID: 2642649491     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050739     Document Type: Article

References (19)

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