Prenatal diagnosis of trisomy 21 without the Down syndrome phenotype

Prenatal Diagnosis

Volumn 26, Issue 12, 2006, Pages 1168-1171

  Aguinaga, M ^a   Razo, G ^a   Castro, J ^a   Mayen Molina D G ^a  

^a INSTITUTO NACIONAL DE PERINATOLOGÍA   (Mexico)

Author keywords

Down syndrome chromosomal region (DSCR); Fluorescence in situ hybridization (FISH); Karyotype; Prenatal diagnosis

Indexed keywords

ANAMNESIS; ARTICLE; BACTERIAL INFECTION; CASE REPORT; CHROMOSOME 20; CHROMOSOME 21; CHROMOSOME ANALYSIS; CLINICAL FEATURE; DISEASE ASSOCIATION; DOWN SYNDROME; DUODENUM ATRESIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE PROBE; GENETIC ANALYSIS; HOSPITAL DISCHARGE; HUMAN; KARYOTYPE 46,XX; MEIOSIS; NEWBORN; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY 21;

ADULT; CHROMOSOMES, HUMAN, PAIR 21; DOWN SYNDROME; DUODENAL OBSTRUCTION; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; LAPAROTOMY; MALE; PEDIGREE; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 33845562934     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1583     Document Type: Article

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