Comments on "congenital diaphragmatic hernia: Is 15q26.1-26.2 a candidate locus?" [8]

American Journal of Medical Genetics

Volumn 131 A, Issue 2, 2004, Pages 224-

  Tönnies, Holger ^a,b  

^a HUMBOLDT UNIVERSITY   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 15Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL DIAPHRAGM HERNIA; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; HUMAN; KARYOTYPE; LETTER; PHENOTYPE; PRIORITY JOURNAL;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; HERNIA, DIAPHRAGMATIC; HUMANS;

EID: 9644303417     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30320     Document Type: Letter

References (5)

1. Biggio JR Jr, Descartes MD, Carroll AJ, Holt RL. 2004. Congenital diaphragmatic hernia: Is 15q26.1-26.2 a candidate locus? Am J Med Genet 126A:183-185.
2. Roback EW, Barakat AJ, Dev VG, Mbikay M, Chretien M, Butler MG. 1991. An infant with deletion of the distal long arm of chromosome 15 (q26.1qter) and loss of insulin-like growth factor I receptor gene. Am J Med Genet 38:74-79.
3. Siebler T, Lopaczynski W, Terry CL, Casella SJ, Munson P, De Leon DD, Phang L, Blakemore KJ, McEvoy RC, Kelley RI, Nissley P. 1995. Insulin-like growth factor I receptor expression and function in fibroblasts from two patients with deletion of the distal long arm of chromosome 15. J Clin Endocrinol Metab 80(12):3447-3457.
4. Tönnies H. 2002. Modern molecular cytogenetic techniques in genetic diagnostics. Trends Mol Med 8(6):246-250.
5. Tönnies H, Schulze I, Hennies H, Neumann LM, Keitzer R, Neitzel H. 2001. De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes. J Med Genet 38(9):617-621.