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Authors: J M Klep-de Pater; J B Bijlsma; E M Bleeker-Wagemakers; H F de France; C M de Vries-Ekkers
Journal: J Med Genet Date: 1979-04 Impact factor: 6.318

3. A girl with karyotype 46,XX,del(7)(pter leads to q32:).

Authors: U Friedrich; O Osterballe; S Stenbjerg; J Jørgensen
Journal: Hum Genet Date: 1979-10-01 Impact factor: 4.132

4. Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.

Authors: K B Nielsen; F Egede; I Mouridsen; J Mohr
Journal: J Med Genet Date: 1979-12 Impact factor: 6.318

5. Assignment of human coagulation factor XII (fXII) to chromosome 5 by cDNA hybridization to DNA from somatic cell hybrids.

Authors: F Citarella; M Tripodi; A Fantoni; F Bernardi; G Romeo; M Rocchi
Journal: Hum Genet Date: 1988-12 Impact factor: 4.132

6. Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8.

Authors: J de Grouchy; M D Dautzenberg; C Turleau; S Beguin; F Chavin-Colin
Journal: Hum Genet Date: 1984 Impact factor: 4.132

7. Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7.

Authors: B Biederman; P Bowen
Journal: Hum Genet Date: 1978-02-23 Impact factor: 4.132

Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band.

1. [Analytical study on Quick test; determination of prothrombin, proconvertin, and proaccelerin].

2. [Coagulation factor VII deficiency in 3 patients with trisomy 8].

3. [A new technic of analysis of the human karyotype].

4. [The human karyotype after treatment with alpha-chymotrypsin].

5. [Effect of the ionic medium on controlled heat denaturation of human chromosomes].

6. Identification of individual chromosomes in the human karyotype by their banding pattern after proteolytic digestion.

7. [Chromosomal studies from cell cultures. Technical modifications].

8. [Probable localisation of a Hageman (factor XII) locus on an autosome].

9. A case of?6p- chromosomal aberration.

1. Nonrandom distribution of exchange points in patients with structural rearrangements.

2. Two cases with different deletions of the long arm of chromosome 7.

3. A girl with karyotype 46,XX,del(7)(pter leads to q32:).

4. Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.

5. Assignment of human coagulation factor XII (fXII) to chromosome 5 by cDNA hybridization to DNA from somatic cell hybrids.

6. Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8.

7. Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7.

8. Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities.

9. A case of partial 5q trisomy associated with partial 7q monosomy.

10. Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter leads to q2200::q3200 leads to qter).