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Clinical Genetics|April 29, 1998
ACTH receptor mutation in a girl with familial glucocorticoid deficiencyA M Slavotinek, J A Hurst, D Dunger, et al.Clinical Genetics|July 3, 1998
Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patientsP C Patsalis, C Sismani, M I Hadjimarcou, et al.Clinical Genetics|July 3, 1998
G2 repair in Nijmegen breakage syndrome: G2 duration and effect of caffeine and cycloheximide in control and X-ray irradiated lymphocytesJ Pincheira, M Bravo, M J SantosClinical Genetics|June 4, 1998
Clinical, morphological and biochemical features in the familial articular hypermobility syndrome (FAHS): a family studyD García-Cruz, S Cano-Colín, J Sánchez-Corona, et al.Clinical Genetics|June 4, 1998
Vascular anastomoses leading to amelia and cutis aplasia in a dizygotic twin pregnancyM C Phelan, J S Geer, W R BlackburnClinical Genetics|June 4, 1998
A case of insertional translocation involving chromosomes 2 and 4A Asamoah, K N Nandi, L Prouty, et al.Clinical Genetics|February 13, 2026
Novel Haplotype-Based Noninvasive Prenatal Diagnosis for Recessive Single-Gene Disorders: A Proof-of-Concept StudyChao Chen, Yaping Zhu, Lu Jiang, et al.Clinical Genetics|November 1, 1985
Tandem duplication of 10(q21-q22) in a mentally deficient manA ReinthallerClinical Genetics|August 26, 2025
RNA Analysis Uncovers Pathogenic PARN Variant in Dyskeratosis CongenitaDaria Akimova, Natalia Semenova, Tatiana Cherevatova, et al.Clinical Genetics|October 1, 1979
Familial congenital diaphragmatic hernia: prenatal diagnostic approach and analysis of twelve familiesJ P CranePageof 719