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Journal of Medical Genetics|September 1, 1996
Attitudes towards cancer predictive testing and transmission of information to the familyC Julian-Reynier, F Eisinger, P Vennin, et al.Journal of Medical Genetics|September 1, 1996
Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndromeM Wang, P Kishnani, M Decker-Phillips, et al.Journal of Medical Genetics|September 1, 1996
Rett syndrome, classical and atypical: genealogical support for common originH O Akesson, B Hagberg, J WahlströmJournal of Medical Genetics|September 1, 1996
A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalitiesL Telvi, A Ion, J C Carel, et al.Journal of Medical Genetics|September 1, 1996
Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testingG Rumsby, A F Massoud, C Avey, et al.Journal of Medical Genetics|February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian familiesM R Passos-Bueno, E S Moreira, S K Marie, et al.Journal of Medical Genetics|February 1, 1996
The genetics of cornea plana congenitaE Tahvanainen, H Forsius, J Kolehmainen, et al.Journal of Medical Genetics|February 1, 1996
Familial psychiatric presentation of Huntington's diseaseS Lovestone, S Hodgson, P Sham, et al.Journal of Medical Genetics|February 1, 1996
Familial adenomatous polyposis in a 5 year old child: a clinical, pathological, and molecular genetic studyS Distante, S Nasioulas, G R Somers, et al.Journal of Medical Genetics|February 1, 1996
Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: a report of a Bedouin babyM A Sabry, D Obenbergerova, R Al-Sawan, et al.Pageof 649