Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks pheno-type

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 66, Issue 1, 1996, Pages 104-112

  Lindeman Kusse, M C ^a,b,f   Van Haeringen, A ^c   Hoorweg Nijman, J J G ^d   Brunner, H G ^e  

^a Institutions the Mentally Disabled   (Netherlands)

^b Institutions the Mentally Disabled   (Netherlands)

^c LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^d VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^e RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^f NONE   (Netherlands)

Author keywords

4p ; Multiple congenital anomalies; Pitt Rogers Danks; Wolf Hirschhorn

Indexed keywords

CANIS;

GROWTH HORMONE; HUMAN GROWTH HORMONE; PHENOBARBITAL; THYROXINE; VALPROIC ACID;

ADOLESCENT; ARTICLE; BONE AGE; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME DELETION 4; CLINICAL TRIAL; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH RETARDATION; HUMAN; MALE; MENTAL DEFICIENCY; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SEIZURE; WOLF HIRSCHHORN SYNDROME;

ABNORMALITIES, MULTIPLE; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 4; FACE; FEMALE; GENE DELETION; GROWTH DISORDERS; HUMANS; MALE; MENTAL RETARDATION; PHENOTYPE; SYNDROME;

EID: 0029857869     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961202)66:1<104::AID-AJMG28>3.0.CO;2-V     Document Type: Article

References (10)

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