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Tijdschrift beschrijving
Alle jaargangen van het bijbehorende tijdschrift
Alle afleveringen van het bijbehorende jaargang
Alle artikelen van de bijbehorende aflevering
54 gevonden resultaten
| nr | titel | auteur | tijdschrift | jaar | jaarg. | afl. | pagina('s) | type |
| 1 | Achondroplasia |
1967 |
70 | 3P2 |
p. 504- 1 p. |
artikel |
||
| 2 | Albright's hereditary osteodystrophy |
1967 |
70 | 3P2 |
p. 494- 1 p. |
artikel |
||
| 3 | Ataxia telangiectasia |
1967 |
70 | 3P2 |
p. 487- 1 p. |
artikel |
||
| 4 | Brachydactyly and spherophakia |
1967 |
70 | 3P2 |
p. 495- 1 p. |
artikel |
||
| 5 | Brachydactyly, peculiar facies, and mental retardation |
1967 |
70 | 3P2 |
p. 496- 1 p. |
artikel |
||
| 6 | Cartilage-hair hypoplasia |
1967 |
70 | 3P2 |
p. 512- 1 p. |
artikel |
||
| 7 | Chondrodystrophia calcificans congenita |
1967 |
70 | 3P2 |
p. 516- 1 p. |
artikel |
||
| 8 | Chondroectodermal dysplasia |
1967 |
70 | 3P2 |
p. 503- 1 p. |
artikel |
||
| 9 | Cleidocranial dysostosis |
1967 |
70 | 3P2 |
p. 500- 1 p. |
artikel |
||
| 10 | Cockayne's syndrome |
1967 |
70 | 3P2 |
p. 489- 1 p. |
artikel |
||
| 11 | Congenital blepharophimosis with generalized myopathy |
1967 |
70 | 3P2 |
p. 492- 1 p. |
artikel |
||
| 12 | Congenital heart disease, deafness, and skeletal malformations |
1967 |
70 | 3P2 |
p. 497- 1 p. |
artikel |
||
| 13 | Congenital rubella |
1967 |
70 | 3P2 |
p. 517- 1 p. |
artikel |
||
| 14 | Cornelia De Lange syndrome |
1967 |
70 | 3P2 |
p. 480- 1 p. |
artikel |
||
| 15 | Cortical thickening of tubular bones |
1967 |
70 | 3P2 |
p. 498- 1 p. |
artikel |
||
| 16 | Cri du chat syndrome |
1967 |
70 | 3P2 |
p. 475- 1 p. |
artikel |
||
| 17 | Diastrophic nanism (Dwarfism) |
1967 |
70 | 3P2 |
p. 502- 1 p. |
artikel |
||
| 18 | Down's syndrome |
1967 |
70 | 3P2 |
p. 474- 1 p. |
artikel |
||
| 19 | Dyschondrostéose of Léri-Weill |
1967 |
70 | 3P2 |
p. 501- 1 p. |
artikel |
||
| 20 | Emotional deprivation and growth retardation simulating true idiopathic hypopituitarism |
1967 |
70 | 3P2 |
p. 470- 1 p. |
artikel |
||
| 21 | Fanconi's syndrome of multiple defects and development of pancytopenia |
1967 |
70 | 3P2 |
p. 479- 1 p. |
artikel |
||
| 22 | Hunter's disease |
1967 |
70 | 3P2 |
p. 509- 1 p. |
artikel |
||
| 23 | Hurler's disease |
1967 |
70 | 3P2 |
p. 508- 1 p. |
artikel |
||
| 24 | Hyperphosphatasia with metaphyseal dysostosis, intestinal malabsorption, anemia plus leukopenia, and fine hair |
1967 |
70 | 3P2 |
p. 513- 1 p. |
artikel |
||
| 25 | Hypophosphatasia |
1967 |
70 | 3P2 |
p. 514- 1 p. |
artikel |
||
| 26 | Hypopituitarism |
1967 |
70 | 3P2 |
p. 468- 1 p. |
artikel |
||
| 27 | Introduction |
Smith, David W. |
1967 |
70 | 3P2 |
p. 463-465 3 p. |
artikel |
|
| 28 | Isolated growth hormone deficiency |
1967 |
70 | 3P2 |
p. 469- 1 p. |
artikel |
||
| 29 | Leprechaunism |
1967 |
70 | 3P2 |
p. 491- 1 p. |
artikel |
||
| 30 | Metaphyseal dysostosis; autosomal dominant type |
1967 |
70 | 3P2 |
p. 511- 1 p. |
artikel |
||
| 31 | Mild congenital hypothyroidism |
1967 |
70 | 3P2 |
p. 467- 1 p. |
artikel |
||
| 32 | Morquio's disease |
1967 |
70 | 3P2 |
p. 507- 1 p. |
artikel |
||
| 33 | Multiple epiphyseal dysplasia |
1967 |
70 | 3P2 |
p. 505- 1 p. |
artikel |
||
| 34 | Oculomandibulodyscephaly with hypotrichosis |
1967 |
70 | 3P2 |
p. 481- 1 p. |
artikel |
||
| 35 | Osteogenesis imperfecta |
1967 |
70 | 3P2 |
p. 515- 1 p. |
artikel |
||
| 36 | Other conditions |
1967 |
70 | 3P2 |
p. 518-519 2 p. |
artikel |
||
| 37 | Peculiar facies and eczema |
1967 |
70 | 3P2 |
p. 486- 1 p. |
artikel |
||
| 38 | Peculiar facies and telangiectatic rash |
1967 |
70 | 3P2 |
p. 485- 1 p. |
artikel |
||
| 39 | Peculiar facies, mental retardation, supravalvular aortic stenosis, infantile hypercalcemia |
1967 |
70 | 3P2 |
p. 493- 1 p. |
artikel |
||
| 40 | Peculiar hair, and focal cerebral and cerebellar degeneration |
1967 |
70 | 3P2 |
p. 488- 1 p. |
artikel |
||
| 41 | Prader-Willi syndrome |
1967 |
70 | 3P2 |
p. 471- 1 p. |
artikel |
||
| 42 | Progeria |
1967 |
70 | 3P2 |
p. 490- 1 p. |
artikel |
||
| 43 | Pyknodysostosis of Maroteaux and Lamy |
1967 |
70 | 3P2 |
p. 499- 1 p. |
artikel |
||
| 44 | Seckel's syndrome |
1967 |
70 | 3P2 |
p. 482- 1 p. |
artikel |
||
| 45 | Severe congenital hypothyroidism |
1967 |
70 | 3P2 |
p. 466- 1 p. |
artikel |
||
| 46 | Silver's syndrome |
1967 |
70 | 3P2 |
p. 483- 1 p. |
artikel |
||
| 47 | Smith-Lemli-Opitz syndrome |
1967 |
70 | 3P2 |
p. 478- 1 p. |
artikel |
||
| 48 | Sporadic cases with prenatal onset of short stature and no recognized syndrome |
1967 |
70 | 3P2 |
p. 484- 1 p. |
artikel |
||
| 49 | The 18 trisomy syndrome |
1967 |
70 | 3P2 |
p. 477- 1 p. |
artikel |
||
| 50 | Turner-like syndrome without X chromosome abnormality |
1967 |
70 | 3P2 |
p. 473- 1 p. |
artikel |
||
| 51 | X-linked hypophosphatemic rickets |
1967 |
70 | 3P2 |
p. 510- 1 p. |
artikel |
||
| 52 | X-linked spondyloepiphyseal dysplasia |
1967 |
70 | 3P2 |
p. 506- 1 p. |
artikel |
||
| 53 | XO turner's syndrome |
1967 |
70 | 3P2 |
p. 472- 1 p. |
artikel |
||
| 54 | XXXXY syndrome |
1967 |
70 | 3P2 |
p. 476- 1 p. |
artikel |
54 gevonden resultaten