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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1970 1
1976 1
1978 1
1979 1
1982 1
1983 1
1984 2
1986 2
1987 1
1988 2
1989 1
1990 2
1991 2
1992 1
1993 2
1994 1
1995 3
1996 3
1997 4
1998 5
1999 4
2001 2
2002 4
2003 1
2004 1
2007 2
2022 0
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51 results
Results by year
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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.
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature.
Luquet I, Mugneret F, Athis PD, Nadal N, Favre B, Abel C, Chelloug N, Lespinasse J, Portnoi MF, Joyé N, Dupont JM, Lebbar A, Bresson JL, Fellmann F, Siffroi JP, Chantot-Bastaraud S, Chiesa J, Amblard F, Devillard F, Jeandidier E, Boceno M, Rival JM, Bellec V, Lallaoui H, Delobel B, Croquette MF, Benzacken B. Luquet I, et al. Among authors: croquette mf. Ann Genet. 2002 Apr-Jun;45(2):77-88. doi: 10.1016/s0003-3995(02)01118-8. Ann Genet. 2002. PMID: 12119216 Review.
Cancer risk in heterozygotes for ataxia-telangiectasia.
Geoffroy-Perez B, Janin N, Ossian K, Laugé A, Croquette MF, Griscelli C, Debré M, Bressac-de-Paillerets B, Aurias A, Stoppa-Lyonnet D, Andrieu N. Geoffroy-Perez B, et al. Among authors: croquette mf. Int J Cancer. 2001 Jul 15;93(2):288-93. doi: 10.1002/ijc.1329. Int J Cancer. 2001. PMID: 11410879 Free article.
[The karyotype of sterile and infertile men].
Croquette MF, Gabriel-Robez O, Couturier J. Croquette MF, et al. Bull Assoc Anat (Nancy). 1987 Dec;71(215):35-9. Bull Assoc Anat (Nancy). 1987. PMID: 3333315 Review. French. No abstract available.
An excess of chromosome 1 breakpoints in male infertility.
Bache I, Assche EV, Cingoz S, Bugge M, Tümer Z, Hjorth M, Lundsteen C, Lespinasse J, Winther K, Niebuhr A, Kalscheuer V, Liebaers I, Bonduelle M, Tournaye H, Ayuso C, Barbi G, Blennow E, Bourrouillou G, Brondum-Nielsen K, Bruun-Petersen G, Croquette MF, Dahoun S, Dallapiccola B, Davison V, Delobel B, Duba HC, Duprez L, Ferguson-Smith M, Fitzpatrick DR, Grace E, Hansmann I, Hultén M, Jensen PK, Jonveaux P, Kristoffersson U, Lopez-Pajares I, McGowan-Jordan J, Murken J, Orera M, Parkin T, Passarge E, Ramos C, Rasmussen K, Schempp W, Schubert R, Schwinger E, Shabtai F, Smith K, Stallings R, Stefanova M, Tranebjerg L, Turleau C, van der Hagen CB, Vekemans M, Vokac NK, Wagner K, Wahlstroem J, Zelante L, Tommerup N. Bache I, et al. Among authors: croquette mf. Eur J Hum Genet. 2004 Dec;12(12):993-1000. doi: 10.1038/sj.ejhg.5201263. Eur J Hum Genet. 2004. PMID: 15367911
The Prader-Willi phenotype of fragile X syndrome.
Nowicki ST, Tassone F, Ono MY, Ferranti J, Croquette MF, Goodlin-Jones B, Hagerman RJ. Nowicki ST, et al. Among authors: croquette mf. J Dev Behav Pediatr. 2007 Apr;28(2):133-8. doi: 10.1097/01.DBP.0000267563.18952.c9. J Dev Behav Pediatr. 2007. PMID: 17435464
[Karyotyping and fetal malformations].
Croquette MF. Croquette MF. Soins Gynecol Obstet Pueric Pediatr. 1984 Apr;(35):24-5. Soins Gynecol Obstet Pueric Pediatr. 1984. PMID: 6564764 French. No abstract available.
51 results