E. Passage

B. Dworniczak, P. Pennekamp, S. Burtey, 2008, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Human plasma inter-alpha-trypsin inhibitor is encoded by four genes on three chromosomes.

Jean‐Pierre Martin, M. Diarra‐Mehrpour, R. Sesboüé, 1989, European journal of biochemistry.

In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13

M. Mattei, D. Ojcius, C. Valentin, 2004, Human Genetics.

Assignment of the human gamma-glutamyl transferase gene to the long arm of chromosome 22

G. Guellaen, M. Mattei, A. Pawlak, 1987, Human Genetics.

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

N. Philip, J. Mandel, M. Mattei, 2004, Human Genetics.

Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridization

M. Mattei, P. Jollès, P. Alliel, 1989, Human Genetics.

The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome

D. Pham‐Dinh, M. Mattei, P. Jollès, 1986, Human Genetics.

In situ hybridization and pulsed-field gel analysis define two major minisatellite loci: 1q23 for minisatellite 33.6 and 7q35-q36 for minisatellite 33.15.

M. Mattei, G. Chimini, B. Jordan, 1989, Genomics.

Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?

A. Poustka, M. Pembrey, L. Villard, 2000, American journal of medical genetics.

Human elastin gene: new evidence for localization to the long arm of chromosome 7.

J. Uitto, M. Mattei, J. Davidson, 1991, American journal of human genetics.

Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndrome.

D. Le Paslier, J. Bachellerie, A. Vignal, 1993, Human molecular genetics.

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.

D. Figarella-Branger, C. Huxley, M. Fontès, 1996, Human molecular genetics.

HumanElastin Gene:New Evidence forLocalization totheLong Arm ofChromosome7

M. Mattei, E. Solomon, D. Black, 1991 .

Use of interspersed repetitive sequences-PCR products for cDNA selection

L. Villard, L. Colleaux, M. Fontès, 1995, Mammalian Genome.

The human calbindin D28k (CALB1) and calretinin (CALB2) genes are located at 8q21.3----q22.1 and 16q22----q23, respectively, suggesting a common duplication with the carbonic anhydrase isozyme loci.

M. Parmentier, M. Mattei, G. Vassart, 1991, Cytogenetics and cell genetics.

Molecular dissection of the Schwann cell specific promoter of the PMP22 gene.

D. Sabéran-Djoneidi, M. Fontès, V. Sanguedolce, 2000, Gene.

Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization

N. Philip, M. Mattei, J. Mattéi, 1988, Human Genetics.

Behavioural profiling of a murine Charcot–Marie–Tooth disease type 1A model

F. Clarac, M. Jamon, M. Fontès, 2001, The European journal of neuroscience.

The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism.

M. Lazdunski, J. Grosgeorge, J. Hugnot, 1997, Genomics.

The gene encoding the large human neurofilament subunit (NF-H) maps to the q121–q131 region on human chromosome 22

D. Pham‐Dinh, M. Mattei, J. Mattéi, 1988, Human Genetics.