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Clinical Genetics|February 1, 1993
De novo t(5p;21q) in a patient previously diagnosed as monosomy 21I López-Pajares, A Martin-Ancel, P Cabello, et al.Clinical Genetics|February 1, 1993
A case of Johanson-Blizzard syndrome complicated by diabetes mellitusK Nagashima, H Yagi, T KuroumeClinical Genetics|February 1, 1996
Identification of two apolipoprotein variants, A-I Karatsu (Tyr 100-->His) and A-I Kurume (His 162-->Gln)K Moriyama, J Sasaki, A Matsunaga, et al.Clinical Genetics|February 1, 1996
An Iranian-Armenian LDLR frameshift mutation causing familial hypercholesterolemiaH K Jensen, L G Jensen, P S Hansen, et al.Clinical Genetics|February 1, 1996
Trisomy 18 mosaicism associated with secondary amenorrhea: ratios of mosaicism in different samples and complicationsS Uehara, Y Obara, T Obara, et al.Clinical Genetics|February 1, 1996
Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndromeD Wieczorek, G Gillessen-Kaesbach, S Plewa, et al.Clinical Genetics|February 1, 1996
Screening for coeliac disease as a possible maternal risk factor for neural tube defectW Dickey, F Stewart, J Nelson, et al.Clinical Genetics|September 1, 1995
Molecular cytogenetic studies of duplication 9q32-->q34.3 inserted into 9q13J W Hou, T R WangClinical Genetics|April 1, 1977
Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 casesA T Tharapel, R L Summitt, R S Wilroy, et al.Clinical Genetics|April 1, 1979
Prenatal diagnosis of severe congenital malformations associated with elevated amniotic fluid alpha-feto proteinJ Chemke, R Nisani, R Kassif, et al.Pageof 718