Genetics beyond mendel: Understanding nontraditional inheritance patterns

Postgraduate Medicine

Volumn 108, Issue 3, 2000, Pages

  Wagstaff, Joseph ^a  

^a UNIVERSITY OF VIRGINIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME ANALYSIS; DIAGNOSTIC ACCURACY; DISEASE TRANSMISSION; EXTRACHROMOSOMAL INHERITANCE; FRAGILE X SYNDROME; GENE MUTATION; GENETIC COUNSELING; GENETIC DISORDER; GENOME; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; INHERITANCE; MOSAICISM; TRINUCLEOTIDE REPEAT; X CHROMOSOME;

EID: 0034282475     PISSN: 00325481     EISSN: None     Source Type: Journal    
DOI: 10.3810/pgm.2000.09.1.1210     Document Type: Article

References (6)

1. Genomic imprinting: Nature and clinical relevance
2. Prader-Willi and Angelman syndromes: Disorders of genomic imprinting
3. Molecular basis of the neurodegenerative disorders
4. Trinucleotide repetition and fragile X syndrome
5. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides
6. Frequency of somatic and germ-line mosaicism in retinoblastoma: Implications for genetic counseling