Osteodysplasty (Melnick and Needles syndrome). Report of a case.

Por Coste, F, Maroteaux, P, Chouraki, L
Publicado em 1968

Proteoglycan populations of baboon (Papio papio) articular cartilage.

Por Stanescu, V, Maroteaux, P, Sobczak, E
Publicado em 1977

Kniest syndrome.

Por Stanescu, V, Stanescu, R, Maroteaux, P
Publicado em 1976

An atypical form of mucolipidosis III.

Por Freisinger, P, Padovani, J C, Maroteaux, P
Publicado em 1992

Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome.

Por Le Merrer, M, Brauner, R, Maroteaux, P
Publicado em 1991

Genochondromatosis.

Por Le Merrer, M, Fressinger, P, Maroteaux, P
Publicado em 1991

Dominant carpotarsal osteochondromatosis.

Por Maroteaux, P, Le Merrer, M, Bensahel, H, Freisinger, P
Publicado em 1993

Recessive metaphyseal dysplasia without hypotrichosis. A syndrome clinically distinct from McKusick cartilage-hair hypoplasia.

Por Verloes, A, Pierard, G E, Le Merrer, M, Maroteaux, P
Publicado em 1990

Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia

Por Odent, S., Loget, P., Le Marec, B., Delezoide, A., Maroteaux, P.
Publicado em 1999

Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndrome.

Por Bonaventure, J, Lasselin, C, Mellier, J, Cohen-Solal, L, Maroteaux, P
Publicado em 1992

Microspherophakia-metaphyseal dysplasia: a 'new' dominantly inherited bone dysplasia with severe eye involvement.

Por Verloes, A, Van Maldergem, L, de Marneffe, P, Dufier, J L, Maroteaux, P
Publicado em 1990

Phalangeal microgeodic syndrome, a case series

Por Toelen, J, Van Ackere, T, Brijs, S, Brijs, A, Eykens, A, Maroteaux, P, Wouters, C
Publicado em 2011

Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?

Por Moog, U, Maroteaux, P, Schrander-Stumpel, C, van Ooij, A, Schrander, J, Fryns, J
Publicado em 1999

Dysplasia spondyloepiphysaria congenita and related generalized skeletal dysplasias among children with severe visual handicaps.

Por Fraser, G. R., Friedmann, A. I., Maroteaux, P., Glen-Bott, A. M., Mittwoch, U.
Publicado em 1969

The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24).

Por Le Merrer, M, Ben Othmane, K, Stanescu, V, Lyonnet, S, Van Maldergem, L, Royer, G, Munnich, A, Maroteaux, P
Publicado em 1992

Clinical and genetic heterogeneity of hypochondroplasia.

Por Rousseau, F, Bonaventure, J, Legeai-Mallet, L, Schmidt, H, Weissenbach, J, Maroteaux, P, Munnich, A, Le Merrer, M
Publicado em 1996

Osteocraniostenosis.

Por Verloes, A, Narcy, F, Grattagliano, B, Delezoide, A L, Guibaud, P, Schaaps, J P, Le Merrer, M, Maroteaux, P
Publicado em 1994

Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux type

Por Faivre, L., Le Merrer, M., Megarbane, A., Gilbert, B., Mortier, G., Cusin, V., Munnich, A., Maroteaux, P., Cormier-Daire, V.
Publicado em 2000

Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3

Por Faivre, L, Le Merrer, M, Al-Gazali, L, Ausems, M, Bitoun, P, Bacq, D, Maroteaux, P, Munnich, A, Cormier-Daire, V
Publicado em 2003

Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chon...

Por Wallis, G A, Rash, B, Sykes, B, Bonaventure, J, Maroteaux, P, Zabel, B, Wynne-Davies, R, Grant, M E, Boot-Handford, R P
Publicado em 1996