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Clinical Genetics|August 1, 1988
Karyotyping urine sediment cells confirms trisomy 12 mosaicism detected at amniocentesisN J Leschot, E J Wilmsen-Linders, H P van Geijn, et al.
Clinical Genetics|February 11, 2018
Characteristics of genetic diseases in consanguineous populations in the genomic era: Lessons from Arab communities in North IsraelS A Shalev
Clinical Genetics|February 11, 2018
Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB geneM L Dentici, A Terracciano, E Bellacchio, et al.
Clinical Genetics|February 13, 2018
Cancer gene-panel testing identifies two loss-of-function alleles in PALB2 and PTENC Avgerinou, F Fostira, P Economopoulou, et al.
Clinical Genetics|April 1, 2018
Clinical implication of FMR1 intermediate alleles in a Spanish populationM I Alvarez-Mora, I Madrigal, F Martinez, et al.
Clinical Genetics|February 1, 1978
Familial syndrome of progressive cone dystrophy, degenerative liver disease, and endocrine dysfunction. III. Genetic studiesK Berg, I F Larsen, E Hansen
Clinical Genetics|November 2, 2019
Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohortHuidan Wu, Honghui Li, Ting Bai, et al.
Clinical Genetics|November 2, 2019
Who should access germline genome sequencing? A mixed methods study of patient viewsMegan C Best, Phyllis Butow, Chris Jacobs, et al.
Clinical Genetics|May 1, 1991
Monozygotic twin girls with diploid/triploid chromosome mosaicism and cutaneous pigmentary dysplasiaE A Wulfsberg, W C Wassel, C A Polo
Clinical Genetics|May 1, 1991
Interstitial deletion of chromosome 2q associated with ovarian dysgenesisE Davis, M Grafe, C Cunniff, et al.
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