Malformation Syndromes in India
Publisher
Springer Netherlands
Reference38 articles.
1. Agarwal SS, Phadke S, Fredund V, Viligeon D, Beighton P (1997) Mselini and Handigodu familial osteoarthropathies: syndromic identity. Am J Med Genet 72: 435–439.
2. Agarwal SS, Phadke SR, Phadke RV, Das SK, Singh GF, Sharma JP, Teotia SRS, Saxena BN (1994) Handigodu disease: a radiological study. A new variety of spondyloepimetaphyseal dysplasia of autosomal dominant type. Skeletal Radiol 23: 611–619.
3. Al Aqueel A, Al Sewairi W, Edress B, Gorlin RJ, Desnick RJ, Martignetti JA (2000) Inherited multicentric osteolysis variant resembling Torg syndrome in a Saudi Family. Am J Med Genet 93: 11–18.
4. Bijarnia S, Baijal A, Verma IC (2003) Genetic Counseling in Acrocallosal syndrome. Indian Pediatrics 70 (2): 169–171.
5. Biswas AC, Reddy A (1997) Images in clinical practice: Progeria. Indian Pediatrics 34 (10): 945–946.