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7 in total

1. An operated case of Holt-Oram syndrome with autosomal dominant inheritance.

Authors: Z Czakó; A Gömöry; P Homolay; S Bacsa; S Kiss; F Móricz; F Fülöp; Z Papp
Journal: Basic Res Cardiol Date: 1976 Jan-Feb Impact factor: 17.165

2. Wilms' tumour and a de novo (1;7) translocation in a child with bilateral radial aplasia.

Authors: M Hewitt; P W Lunt; A Oakhill
Journal: J Med Genet Date: 1991-06 Impact factor: 6.318

3. The Holt-Oram syndrome.

Authors: J A Hurst; C M Hall; M Baraitser
Journal: J Med Genet Date: 1991-06 Impact factor: 6.318

4. Partial trisomy 4q due to familial 2/4 translocation.

Authors: B Biederman; P Bowen
Journal: Hum Genet Date: 1976-07-27 Impact factor: 4.132

5. A child with multiple congenital malformations and a 46,XX,t(Bq+;Dq-)-45,XX,-B,-D,+der(B),t(Bq+;Dq-) karyotype.

Authors: A Carnevale; L De los Cobos
Journal: J Med Genet Date: 1973-12 Impact factor: 6.318

6. Holt Oram syndrome mistaken for thalidomide embryopathy--embryological considerations.

Authors: N Van Regemorter; D Haumont; C Kirkpatrick; P Viseur; P Jeanty; J Dodion; J Milaire; M Rooze; F Rodesch
Journal: Eur J Pediatr Date: 1982-02 Impact factor: 3.183

7. Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion.

Authors: S J Funderburk; B F Crandall
Journal: Am J Hum Genet Date: 1974-11 Impact factor: 11.025

7 in total