A case with de novo interstitial deletion of chromosome 7q21.1-q22

Genetic Counseling

Volumn 16, Issue 2, 2005, Pages 155-159

  Manguoglu E ^a   Berker Karaüzüm, Sibel ^a   Baumer, A ^a   Mihci E ^b   Tacoy S ^b   Luleci G ^a   Schinzel, A ^a  

^a AKDENIZ UNIVERSITY   (Turkey)

^b Institute of Medical Genetics   (Switzerland)

Author keywords

7q21.1 q22; Interstitial deletion

Indexed keywords

ARTICLE; ASTIGMATISM; CASE REPORT; CHROMOSOME 7Q; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CLINICAL FEATURE; CLINODACTYLY; CONGENITAL MALFORMATION; CYTOGENETICS; DIVERGENT STRABISMUS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH RETARDATION; HUMAN; HYPERMETROPIA; HYPOTELORISM; KARYOTYPE; MENTAL DEFICIENCY; MICROCEPHALY; MOLECULAR GENETICS; PALPEBRAL FISSURE ANOMALY; SCHOOL CHILD; SPASTICITY; WILLIAMS BEUREN SYNDROME;

ABNORMALITIES, MULTIPLE; BACLOFEN; CHILD; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 7; DEVELOPMENTAL DISABILITIES; FEMALE; GENITALIA, FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE;

EID: 22444451239     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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