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Delineation of two distinct 6p deletion syndromes.

(1999) HUMAN GENETICS. 104(1). p.64-72
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Chicago
DAVIES, AF, G MIRZA, G SEKHON, P TURNPENNY, F LEROY, Franki Speleman, C LAW, et al. 1999. “Delineation of Two Distinct 6p Deletion Syndromes.” Human Genetics 104 (1): 64–72.
APA
DAVIES, A., MIRZA, G., SEKHON, G., TURNPENNY, P., LEROY, F., Speleman, F., LAW, C., et al. (1999). Delineation of two distinct 6p deletion syndromes. HUMAN GENETICS, 104(1), 64–72.
Vancouver
1.
DAVIES A, MIRZA G, SEKHON G, TURNPENNY P, LEROY F, Speleman F, et al. Delineation of two distinct 6p deletion syndromes. HUMAN GENETICS. 1999;104(1):64–72.
MLA
DAVIES, AF, G MIRZA, G SEKHON, et al. “Delineation of Two Distinct 6p Deletion Syndromes.” HUMAN GENETICS 104.1 (1999): 64–72. Print.
@article{174113,
  author       = {DAVIES, AF and MIRZA, G and SEKHON, G and TURNPENNY, P and LEROY, F and Speleman, Franki and LAW, C and VAN REGEMORTER, N and VAMOS, E and FLINTER, F and RAGOUSSIS, J},
  issn         = {0340-6717},
  journal      = {HUMAN GENETICS},
  language     = {eng},
  number       = {1},
  pages        = {64--72},
  title        = {Delineation of two distinct 6p deletion syndromes.},
  volume       = {104},
  year         = {1999},
}

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