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Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations.

(1997) HUMAN MOLECULAR GENETICS. 6(1). p.91-98
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Chicago
MEYER, J, P SUDBECK, M HELD, T WAGNER, ML SCHMITZ, FD BRICARELLI, E EGGERMONT, et al. 1997. “Mutational Analysis of the SOX9 Gene in Campomelic Dysplasia and Autosomal Sex Reversal: Lack of Genotype/phenotype Correlations.” Human Molecular Genetics 6 (1): 91–98.
APA
MEYER, J., SUDBECK, P., HELD, M., WAGNER, T., SCHMITZ, M., BRICARELLI, F., EGGERMONT, E., et al. (1997). Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations. HUMAN MOLECULAR GENETICS, 6(1), 91–98.
Vancouver
1.
MEYER J, SUDBECK P, HELD M, WAGNER T, SCHMITZ M, BRICARELLI F, et al. Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations. HUMAN MOLECULAR GENETICS. 1997;6(1):91–8.
MLA
MEYER, J, P SUDBECK, M HELD, et al. “Mutational Analysis of the SOX9 Gene in Campomelic Dysplasia and Autosomal Sex Reversal: Lack of Genotype/phenotype Correlations.” HUMAN MOLECULAR GENETICS 6.1 (1997): 91–98. Print.
@article{181921,
  author       = {MEYER, J and SUDBECK, P and HELD, M and WAGNER, T and SCHMITZ, ML and BRICARELLI, FD and EGGERMONT, E and FRIEDRICH, U and HAAS, OA and KOBELT, A and Leroy, Juliaan and VANMALDERGEM, L and MICHEL, E and MITULLA, B and PFEIFFER, RA and SCHINZEL, A and SCHMIDT, H and SCHERER, G},
  issn         = {0964-6906},
  journal      = {HUMAN MOLECULAR GENETICS},
  language     = {eng},
  number       = {1},
  pages        = {91--98},
  title        = {Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations.},
  volume       = {6},
  year         = {1997},
}