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American Journal of Medical Genetics|November 15, 1992
Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33-qterF H Menko, K Madan, J A Baart, et al.American Journal of Medical Genetics|February 1, 1992
Gelsolin gene mutation--at codon 187--in familial amyloidosis, Finnish: DNA-diagnostic assayM Haltia, E Levy, J Meretoja, et al.American Journal of Medical Genetics|March 11, 1992
Birth prevalence study of the Apert syndromeM M Cohen, S Kreiborg, E J Lammer, et al.American Journal of Medical Genetics|February 15, 1992
Variability in the clinical and pathological findings in the neuronal ceroid lipofuscinoses: review of data and observationsK E Wisneiwski, E Kida, O F Patxot, et al.American Journal of Medical Genetics|September 15, 1992
Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literatureC L Garganta, J N BodurthaAmerican Journal of Medical Genetics|September 15, 1992
Further delineation of the Simpson-Golabi-Behmel (SGB) syndromeF Gurrieri, M Cappa, G NeriAmerican Journal of Medical Genetics|September 15, 1992
Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infantP J Gillar, C I Kaye, S G Ryan, et al.American Journal of Medical Genetics|September 15, 1992
Experimental fetal alcohol syndrome: proposed pathogenic basis for a variety of associated facial and brain anomaliesL E Kotch, K K SulikAmerican Journal of Medical Genetics|September 15, 1992
Natural history of mosaic trisomy 14 syndromeA Fujimoto, J Allanson, C A Crowe, et al.American Journal of Medical Genetics|September 15, 1992
Esophageal atresia and tracheoesophageal fistula in two infants born to hyperthyroid women receiving methimazole (Tapazol) during pregnancyA Ramírez, A Espinosa de los Monteros, A Parra, et al.Pageof 854