Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome [2]

American Journal of Medical Genetics

Volumn 109, Issue 3, 2002, Pages 234-237

  Marti, Zoltn ^a   Kutsche, Kerstin ^a,d   Sutajova, Marketa ^a   Gal, Andreas ^b   Nothwang, Hans Gerd ^b   Czeizel, Andrew E ^c   Tmr, Lszl ^c   Slyom, Enik ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^c OKK Csaldtervezsi Kzpont   (Hungary)

^d Borsod County Teaching Hospital   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL ARTIFICIAL CHROMOSOME; CHROMOSOME 12Q; CHROMOSOME 1Q; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION 22; COSTELLO SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LETTER; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

BACTERIA (MICROORGANISMS);

EID: 0036568959     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10314     Document Type: Letter

References (7)

1. Male to male transmission of Costello syndrome consistent with autosomal dominant inheritence
2. A new syndrome
3. A new syndrome: Mental subnormality and nasal papillomata
4. Hungarian case with Costello syndrome and translocation t(1,22)
5. Cloning and characterization of the breakpoint regions of - A chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium
6. Genetics of the Costello syndrome
7. Costello syndrome with acoustic neuroma and cataract. Is the Costello locus linked to neurofibromatosis type 2 on 22q?