The 6p subtelomere deletion syndrome

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 145, Issue 4, 2007, Pages 377-382

  DeScipio, Cheryl ^a  

^a BELLEVUE HOSPITAL CENTER   (United States)

Author keywords

3C syndrome; 6p25 subtelomeric deletion; Deletion; Ritscher Schinzel syndrome; Subtelomere

Indexed keywords

ARTICLE; CHROMOSOME 6P; CHROMOSOME DELETION; CHROMOSOME DELETION 6P; CHROMOSOME MAP; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; EYE MALFORMATION; HEARING LOSS; HUMAN; LANGUAGE DISABILITY; MENTAL DEFICIENCY; PHENOTYPE; PRIORITY JOURNAL; SYNDROME; TELOMERE;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 6; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PHENOTYPE; SYNDROME; TELOMERE;

EID: 36348969388     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.30156     Document Type: Article

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