Frontonasal dysplasia, congenital heart defect, and short stature: a further observation.

Por Meinecke, P, Blunck, W
Publicado em 1989

Orofaciodigital syndrome type IV (Mohr-Majewski syndrome) with severe expression expanding the known spectrum of anomalies.

Por Meinecke, P, Hayek, H
Publicado em 1990

Microcephalic osteodysplastic primordial dwarfism type I/III in sibs.

Por Meinecke, P, Passarge, E
Publicado em 1991

Multiple malformation syndrome including cleft lip and palate and cardiac abnormalities due to an interstitial deletion of chromosome 12q.

Por Meinecke, P, Meinecke, R
Publicado em 1987

Fetal brain disruption sequence: a milder variant.

Por Bönnemann, C G, Meinecke, P
Publicado em 1990

Limb anomalies in the CHARGE association.

Por Meinecke, P, Polke, A, Schmiegelow, P
Publicado em 1989

Balanced t(6;8)(6p8p;6q8q) and the CHARGE association.

Por Hurst, J A, Meinecke, P, Baraitser, M
Publicado em 1991

Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct en...

Por Bönnemann, C G, Meinecke, P, Reich, H
Publicado em 1991

Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation: a new syndrome?

Por Zerres, K, Rietschel, M, Rietschel, E, Majewski, F, Meinecke, P
Publicado em 1992

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS)

Por WIECZOREK, D., KRAUSE, M., MAJEWSKI, F., ALBRECHT, B., MEINECKE, P., RIESS, O., GILLESSEN-KAESBAC..., G.
Publicado em 2000

Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP

Por Bartsch, O, Locher, K, Meinecke, P, Kress, W, Seemanova, E, Wagner, A, Ostermann, K, Rodel, G
Publicado em 2002

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm...

Por Bartsch, O., Wuyts, W., Van Hul, W., Hecht, J. T., Meinecke, P., Hogue, D., Werner, W., Zabel, B., Hinkel, G. K., Powell, C. M., Shaffer, L. G., Willems, P. J.
Publicado em 1996

Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome

Por Seifert, W, Holder‐Espinasse, M, Spranger, S, Hoeltzenbein, M, Rossier, E, Dollfus, H, Lacombe, D, Verloes, A, Chrzanowska, K H, Maegawa, G H B, Chitayat, D, Kotzot, D, Huhle, D, Meinecke, P, Albrecht, B, Mathijssen, I, Leheup, B, Raile, K, Hennies, H C, Horn, D
Publicado em 2006

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.

Por Buiting, K, Dittrich, B, Gross, S, Lich, C, Färber, C, Buchholz, T, Smith, E, Reis, A, Bürger, J, Nöthen, M M, Barth-Witte, U, Janssen, B, Abeliovich, D, Lerer, I, van den Ouweland, A M, Halley, D J, Schrander-Stumpel, C, Smeets, H, Meinecke, P, Malcolm, S, Gardner, A, Lalande, M, Nicholls, R D, Friend, K, Schulze, A, Matthijs, G, Kokkonen, H, Hilbert, P, Van Maldergem, L, Glover, G, Carbonell, P, Willems, P, Gillessen-Kaesbach, G, Horsthemke, B
Publicado em 1998

Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

Por Lüdecke, H.-J., Schaper, J., Meinecke, P., Momeni, P., Groß, S., von Holtum, D., Hirche, H., Abramowicz, M. J., Albrecht, B., Apacik, C., Christen, H.-J., Claussen, U., Devriendt, K., Fastnacht, E., Forderer, A., Friedrich, U., Goodship, T. H. J., Greiwe, M., Hamm, H., Hennekam, R. C. M., Hinkel, G. K., Hoeltzenbein, M., Kayserili, H., Majewski, F., Mathieu, M., McLeod, R., Midro, A. T., Moog, U., Nagai, T., Niikawa, N., Ørstavik, K. H., Plöchl, E., Seitz, C., Schmidtke, J., Tranebjærg, L., Tsukahara, M., Wittwer, B., Zabel, B., Gillessen-Kaesbach, G., Horsthemke, B.
Publicado em 2001