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Journal of Medical Genetics|March 1, 1995
Male neonatal death and progressive weakness and immune deficiency in females: an unknown X linked conditionG Woods, G Black, G NorburyJournal of Medical Genetics|March 1, 1995
A gene for familial venous malformations maps to chromosome 9p in a second large kindredC J Gallione, K A Pasyk, L M Boon, et al.Journal of Medical Genetics|March 1, 1995
Absence of linkage between familial neural tube defects and PAX3 geneS Chatkupt, F A Hol, Y Y Shugart, et al.Journal of Medical Genetics|March 1, 1995
Familial schizencephaly: further delineation of a rare disorderF Haverkamp, K Zerres, B Ostertun, et al.Journal of Medical Genetics|November 1, 1994
Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndromeL H Seaver, J W Pierpont, R P Erickson, et al.Journal of Medical Genetics|November 1, 1994
Deletions in the 5' region of dystrophin and resulting phenotypesF Muntoni, P Gobbi, C Sewry, et al.Journal of Medical Genetics|November 1, 1994
Trinucleotide repeat length and progression of illness in Huntington's diseaseK Kieburtz, M MacDonald, C Shih, et al.Journal of Medical Genetics|November 1, 1994
APC mutation associated with late onset of familial adenomatous polyposisJ Smith-Ravin, K Pack, S Hodgson, et al.Journal of Medical Genetics|October 1, 1994
A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasiaG Calabrese, P G Franchi, L Stuppia, et al.Journal of Medical Genetics|October 1, 1994
Down-Turner syndrome: case report and reviewG J Van Buggenhout, B C Hamel, J C Trommelen, et al.Pageof 649