Euchromatic variant 16p+. Implications in prenatal diagnosis

Prenatal Diagnosis

Volumn 26, Issue 6, 2006, Pages 535-538

  Lopez Pajares I ^a   Villa, O ^b   Salido, M ^b   Mori, M A ^a   Gonzalez, A ^a   Lapunzina, P ^a   De Torres, M L ^a   Vallcorba, I ^a   Palomares, M ^a   Fernandez L ^a   Delicado, A ^a  

^a HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

^b HOSPITAL DEL MAR   (Spain)

Author keywords

Euchromatic heteromorphism; Euchromatic variant 16p+; Fluorescence in situ hybridisation (FISH); Prenatal diagnosis

Indexed keywords

CHLORIDE; CREATINE; SODIUM;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 16P; CHROMOSOME VARIANT; CLINICAL FEATURE; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ADULT; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 16; EUCHROMATIN; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 33745594649     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1454     Document Type: Article

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