Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndrome

Journal of Medical Genetics

Volumn 34, Issue 6, 1997, Pages 441-446

  Kang, Seongman ^a   Allen, Jeffrey ^c   Graham Jr , John M ^d   Grebe, Theresa ^e   Clericuzio, Carol ^f   Patronas, Nicholas ^b   Ondrey, Frank ^b   Green, Eric ^a   Schäffer, Alejandro ^a   Abbott, Margaret ^g   Biesecker, Leslie G ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

^c BETH ISRAEL MEDICAL CENTER   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF ARIZONA   (United States)

^f UNIVERSITY OF NEW MEXICO SCHOOL OF MEDICINE   (United States)

^g JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Epiglottis; Hypothalamic hamartoma; Linkage mapping; Polydactyly

Indexed keywords

ANUS ATRESIA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CHROMOSOME 7P; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; ENDOSCOPY; FAMILY; FEMALE; GENE DELETION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE TRANSLOCATION; GENETIC LINKAGE; HAMARTOMA; HUMAN; HUMAN CELL; LARYNX DISORDER; MAJOR CLINICAL STUDY; MALE; MORBIDITY; PALLISTER HALL SYNDROME; PHENOTYPE; POLYDACTYLY; PRIORITY JOURNAL; RADIOGRAPHY;

EID: 16944362285     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.34.6.441     Document Type: Article

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