B. Noel

发表

Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21

J. Delabar, Z. Rahmani, D. Theophile, 1993, European journal of human genetics : EJHG.

Confirmation of Y/autosome translocations using recombinant DNA

B. Noel, H. Cooke, 2004, Human Genetics.

Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.

C. Junien, C. Lavedan, M. Rethoré, 1989, Cytogenetics and cell genetics.

Characterization of the supernumerary chromosome in cat eye syndrome.

H. McDermid, J. Burn, A. Duncan, 1986, Science.

A deletion map of the human Y chromosome based on DNA hybridization.

D. Botstein, J. Weissenbach, L. Brown, 1986, American journal of human genetics.

A familial Y/autosome translocation in man

I. Emerit, B. Noel, J. Luciani, 1971, Clinical genetics.

[Male pseudohermaphroditism and mosaicism 45,X-46,XYdic-46,XXq-].

B. Noel, B. Quack, R. Boschetti, 1968, Annales de genetique.

Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations

M. Rethoré, B. Noel, B. Quack, 1976, Clinical genetics.

Wolf's syndrome in twins -- translocation in the mother.

B. Noel, D. Viola, M. Levy, 1976, Acta geneticae medicae et gemellologiae.

Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation

B. Noel, A. Chandley, R. Speed, 1990, Human Genetics.

The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families

A. Robinson, Y. Fukushima, N. Niikawa, 2004, Human Genetics.

The 11q;22q translocation: A European collaborative analysis of 43 cases

C. E. Ford, G. Gimelli, A. Hagemeijer, 2004, Human Genetics.

7 cases of trisomy 2q 34 to 2q ter resulting from a familial translocation 2 8 q 34 p 23

B. Noel, J. Guillot, C. Laurent, 1978 .

[Partial trisomy of the long arm of the chromosme 11 by malsegregation of a maternal translocation t(11;22)(q23 1;q1 11)].

M. Rethoré, B. Noel, M. Levy, 1976, Annales de genetique.

Partial 4q trisomy. Apropos of 3 cases.

B. Dutrillaux, B. Noel, A. Forabosco, 1975, Annales de genetique.

Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level.

J. Delabar, Z. Rahmani, D. Theophile, 1994, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

The XY chromosome pair in mouse and human spermatocytes, visualised by silver staining

B. Noel, B. Quack, 1977, Nature.

Meiotic analysis of two human reciprocal X-autosome translocations.

B. Noel, A. Chandley, R. Speed, 1988, Cytogenetics and cell genetics.

[Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].

B. Noel, D. Raudrant, D. Ayral, 1984, Pediatrie.

Molecular mapping of the Down syndrome phenotype on chromosome 21.

J. Delabar, Z. Rahmani, D. Theophile, 1993, Progress in clinical and biological research.

[Trial classification of D group chromosome long arm deletions. Apropos of a 15q- case].

B. Noel, C. Laurent, M. David, 1971, Annales de genetique.

Short arm deletion of chromosome 14

I. Emerit, M. Thiriet, B. Noel, 2004, Humangenetik.

[Complexe de novo rearrangement involving 4 chromosomes in a newborn infant].

B. Noel, J. Martinetti, 1973, Annales de Genetique.