Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies.

American journal of medical genetics. Part A

Volumn 131, Issue 3, 2004, Pages 265-372

  Ehling, Daniela ^a   Kennerknecht, Ingo ^a   Junge, Annelore ^a   Prager, Bettina ^a   Exeler, Rita ^a   Behre, Beate ^a   Horst, Juergen ^a   Schmitt John, Thomas ^a   Bartsch, Oliver ^a   Wirth, Jutta ^a  

^a Praenadia GmbH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PRIMER DNA;

ARTICLE; CASE REPORT; CHROMOSOME 21; CHROMOSOME DELETION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPING; MALE; MONOSOMY; NEWBORN; NUCLEOTIDE SEQUENCE; PHENOTYPE;

BASE SEQUENCE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 21; DNA PRIMERS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; MONOSOMY; PHENOTYPE;

EID: 21644479922     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30361     Document Type: Article

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