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Page 1
[Smith-Magenis syndrome].
Livet MO, Moncla A, Delobel B, Croquette MF, Philip N, Vallée L. Livet MO, et al. Among authors: croquette mf. Arch Pediatr. 1997 Dec;4(12):1231-7. doi: 10.1016/s0929-693x(97)82615-2. Arch Pediatr. 1997. PMID: 9538429 French.
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children).
Mathieu M, Piussan C, Thepot F, Gouget A, Lacombe D, Pedespan JM, Serville F, Fontan D, Ruffie M, Nivelon-Chevallier A, Amblard F, Chauveau P, Moirot H, Chabrolle JP, Croquette MF, Teyssier M, Plauchu H, Pelissier MC, Gilgenkrantz S, Turc-Carel C, Turleau C, Prieur M, Le Merrer M, Gonzales M, Journel H, et al. Mathieu M, et al. Among authors: croquette mf. Ann Genet. 1997;40(1):45-54. Ann Genet. 1997. PMID: 9150850
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations.
Luciani JJ, de Mas P, Depetris D, Mignon-Ravix C, Bottani A, Prieur M, Jonveaux P, Philippe A, Bourrouillou G, de Martinville B, Delobel B, Vallee L, Croquette MF, Mattei MG. Luciani JJ, et al. Among authors: croquette mf. J Med Genet. 2003 Sep;40(9):690-6. doi: 10.1136/jmg.40.9.690. J Med Genet. 2003. PMID: 12960216 Free PMC article. No abstract available.
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene.
Vincent C, Kalatzis V, Compain S, Levilliers J, Slim R, Graia F, Pereira ML, Nivelon A, Croquette MF, Lacombe D, et al. Vincent C, et al. Among authors: croquette mf. Hum Mol Genet. 1994 Oct;3(10):1859-66. doi: 10.1093/hmg/3.10.1859. Hum Mol Genet. 1994. PMID: 7849713
Molecular mapping of a Yq deletion in a patient with normal stature.
Rousseaux-Prévost R, Rigot JM, Delobel B, Lesur P, Collier F, Croquette MF, Gauthier A, Mazeman E, Rousseaux J. Rousseaux-Prévost R, et al. Among authors: croquette mf. Hum Genet. 1996 Oct;98(4):505-7. doi: 10.1007/s004390050248. Hum Genet. 1996. PMID: 8792831
55 results