共 27 条
- [21] Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocation AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 100 (01): : 85 - 86
- [24] The chromosome 21 transcript map: How far from completion with more than 3,000 ESTs. Impact for the molecular genetics of Down syndrome CYTOGENETICS AND CELL GENETICS, 1997, 77 : 13 - 14
- [25] FAMILIAL D/D TRANSLOCATION - A FAMILY SHOWING TRANSMISSION THROUGH 3 GENERATIONS - A CASE WITH MULTIPLE CONGENITAL MALFORMATIONS AND A CASE OF REGULAR 21-TRISOMIC DOWNS SYNDROME ACTA PATHOLOGICA ET MICROBIOLOGICA SCANDINAVICA, 1969, 75 (04): : 545 - &
- [27] MENTAL RETARDATION IN CRI-DU-CHAT-SYNDROME - COMPARISON OF INTELLECTUAL LEVELS IN PARTIAL DELETION OF SHORT ARM OF CHROMOSOMES 5 WITH TRISOMY-21 AND DELETIONS OF CHROMOSOME-18 - 118 CASES FROM LITERATURE REVUE DE NEUROPSYCHIATRIE INFANTILE ET D HYGIENE MENTALE DE L ENFANCE, 1968, 16 (03): : 257 - 267