C. Reid

发表

Saethre-Chotzen syndrome with familial translocation at chromosome 7p22.

E. Zackai, E. Jabs, F. Ramos, 1993, American journal of medical genetics.

An angel with Down syndrome in a sixteenth century Flemish Nativity painting

C. Reid, A. Levitas, Andrew S. Levitas, 2003, American journal of medical genetics. Part A.

Further delineation of spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type, with emphasis on diagnostic features.

J. Lubicky, D. Schidlow, C. Scott, 1993, American journal of medical genetics.

Growth of the foramen magnum in achondroplasia.

R. Pyeritz, J. Hecht, W. Horton, 1989, American journal of medical genetics.

Standard curves of chest circumference in achondroplasia and the relationship of chest circumference to respiratory problems.

R. Pauli, A. Hunter, C. Scott, 1996, American journal of medical genetics.

Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.

L. Jackson, R. Wallerstein, B. Hay, 1997, Journal of medical genetics.

Two craniosynostotic patients with 11q deletions, and review of 48 cases.

E. Jabs, A. Lewanda, C. Reid, 1995, American journal of medical genetics.

Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20).

J. Ott, T. Lehner, B. Gold, 1995, American journal of medical genetics.

Study of two patients with craniosynostosis and deletions of 11q: One with features of Saethre-Chotzen syndrome and the other with concomitant partial trisomy 4q

A. Lewanda, C. Reid, S. Morsey, 1994 .

Rubinstein-Taybi syndrome and psychiatric disorders.

C. Reid, A. Levitas, 2002, Journal of intellectual disability research : JIDR.

Acute lymphoblastic leukemia in a child with the CHIME neuroectodermal dysplasia syndrome.

R. Schnur, W. Heymann, C. Reid, 1997, American journal of medical genetics.