Progress in the autosomal segmental aneusomy syndromes (SASs): Single or multi-locus disorders?

Human Molecular Genetics

Volumn 6, Issue 10 REV. ISS., 1997, Pages 1657-1665

  Budarf, Marcia L ^a   Emanuel, Beverly S ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CONTIG;

ALAGILLE SYNDROME; ARTICLE; AUTOSOMAL DISORDER; CHONDRODYSPLASIA; CHROMOSOMAL LOCALIZATION; CHROMOSOME 22Q; DELETION MUTANT; DIGEORGE SYNDROME; GENE LOCUS; GENE MUTATION; HAPPY PUPPET SYNDROME; HUMAN; INTERSTITIAL CHROMOSOME DELETION; MOUSE; NONHUMAN; PATHOGENESIS; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME; WILLIAMS BEUREN SYNDROME;

ABNORMALITIES, MULTIPLE; ANEUPLOIDY; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN; CHROMOSOMES, HUMAN, PAIR 22; GENE DELETION; GENETIC MARKERS; HUMANS; SYNDROME;

ACRONICTA LEPORINA;

EID: 0030756674     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.10.1657     Document Type: Article

References (7)

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6. Watson,G.H. and Miller,V. (1973) Arteriohepatic dysplasia, familial pulmonary arterial stenosis with neonatal liver disease. Arch. Dis. Childhood 48, 459-466.
7. Krantz,I., Piccoli,D.A. and Spinner,N.B. (1997) Alagille syndrome. J. Med. Genet. 34, 1-6.