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Genetic Counseling (Geneva, Switzerland)|October 28, 2011
Lethal evolution of a newborn with consistent features of hydrolethalus syndrome--Romanian patientV Belengeanu, H Viskari, J Tallila, et al.
Clinical Genetics|June 1, 1993
Marden-Walker syndrome: case report, literature review and nosologic discussionC Schrander-Stumpel, C de Die-Smulders, M de Krom, et al.
Annals of Neurology|October 23, 1997
The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigreesS Claes, K Devriendt, L Lagae, et al.
Patient Education and Counseling|June 24, 2000
Psychosocial problems, coping strategies, and the need for information of parents of children with Prader-Willi syndrome and Angelman syndromeH W van den Borne, R H van Hooren, M van Gestel, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|September 22, 2001
A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 gene cluster on chromosome 13q32M Veugelers, B De Cat, N Delande, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriersA S Plomp, C E De Die-Smulders, P Meinecke, et al.
American Journal of Medical Genetics. Part A|September 11, 2003
Rett syndrome in adolescent and adult females: clinical and molecular genetic findingsE Smeets, E Schollen, U Moog, et al.
Acta Clinica Belgica|August 4, 2007
Intravascular large B-cell lymphoma of the uterus presenting as fever of unknown origin (FUO) and revealed by FDG-PETL Lannoo, S Smets, E Steenkiste, et al.
Gynecologic and Obstetric Investigation|June 19, 2010
Primary retroperitoneal mucinous cystadenocarcinoma: a case report and review of the literatureI Dierickx, G Jacomen, V Schelfhout, et al.
Hepatology (Baltimore, Md.)|November 1, 1988
The development of the intrahepatic bile ducts in man: a keratin-immunohistochemical studyP Van Eyken, R Sciot, F Callea, et al.
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