Diaphragmatic Hernia in 18p- Syndrome [3]

American Journal of Medical Genetics

Volumn 125 A, Issue 1, 2004, Pages 97-99

  Strenge, Sibylle ^a   Froster, Ursula G ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 18P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL DIAPHRAGM HERNIA; DISEASE COURSE; FACE DYSMORPHIA; FEMALE; GENETIC VARIABILITY; GROWTH RETARDATION; HUMAN; LETTER; MALFORMATION SYNDROME; MICROCEPHALY; OLIGOHYDRAMNIOS; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; TRISOMY 13; TRISOMY 18; WEBBED NECK;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; HERNIA, DIAPHRAGMATIC; HUMANS; INFANT; KARYOTYPING; SYNDROME;

EID: 0842327211     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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