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Literature DB >> 5801472

Congenital malformations associated with a ring 4 chromosome.

R Carter, E Baker, D Hayman.

Abstract

Entities: Disease

Mesh：

Year: 1969 PMID： 5801472 PMCID： PMC1468864 DOI： 10.1136/jmg.6.2.224

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

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11 in total

1. DELETION ON SHORT ARMS OF A B-CHROMOSOME WITHOUT "CRI DU CHAT" SYNDROME.

Authors: U WOLF; R PORSCH; H BAITSCH; H REINWEIN
Journal: Lancet Date: 1965-04-03 Impact factor: 79.321

2. Persistent chromosome aberrations in irradiated human subjects.

Authors: M A BENDER; P C GOOCH
Journal: Radiat Res Date: 1962-01 Impact factor: 2.841

3. X-ray-induced chromosome damage in man.

Authors: I M TOUGH; K E BUCKTON; A G BAIKIE; W M COURT-BROWN
Journal: Lancet Date: 1960-10-15 Impact factor: 79.321

4. Deleted late-replicating chromosomes.

Authors: O J Miller; W R Breg; D Warburton; D A Miller; A DeCapoa; A M Chutorian
Journal: Lancet Date: 1966-07-09 Impact factor: 79.321

5. Ring chromosome 18 in a patient with multiple anomalies.

Authors: C G Palmer; N Fareed; A D Merritt
Journal: J Med Genet Date: 1967-06 Impact factor: 6.318

6. Chromosomal findings in two cases of acute erythro-leukaemia.

Authors: M K Jensen
Journal: Acta Med Scand Date: 1966-08

7. "Cri du Chat" due to a ring-B chromosome.

Authors: R A Rohde; R Tompkins
Journal: Lancet Date: 1965-11-20 Impact factor: 79.321

8. Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.

Authors: K Hirschhorn; H L Cooper; I L Firschein
Journal: Humangenetik Date: 1965

9. Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome.

Authors: O J Miller; W R Breg; D Warburton; D A Miller; I L Firschein; K Hirschhorn
Journal: Cytogenetics Date: 1966

10. New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies.

Authors: J C Leão; G J Bargman; R L Neu; T Kajii; L I Gardner
Journal: JAMA Date: 1967-10-30 Impact factor: 56.272

16 in total

1. Derivative chromosomal structures from a ring chromsome 4.

Authors: R Niss; E Passarge
Journal: Humangenetik Date: 1975-05-26

Review 2. Wolf syndrome.

Authors: D S Katz; T H Smith
Journal: Pediatr Radiol Date: 1991

Congenital malformations associated with a ring 4 chromosome.

1. DELETION ON SHORT ARMS OF A B-CHROMOSOME WITHOUT "CRI DU CHAT" SYNDROME.

2. Persistent chromosome aberrations in irradiated human subjects.

3. X-ray-induced chromosome damage in man.

4. Deleted late-replicating chromosomes.

5. Ring chromosome 18 in a patient with multiple anomalies.

6. Chromosomal findings in two cases of acute erythro-leukaemia.

7. "Cri du Chat" due to a ring-B chromosome.

8. Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.

9. Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome.

10. New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies.

1. Derivative chromosomal structures from a ring chromsome 4.

Review 2. Wolf syndrome.

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

4. Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies.

5. The 4p-syndrome, with a report of two new cases.

6. A complex chromosomal rearrangement with formation of a ring 4.

7. A ring-4 chromosome in a patient with normal intelligence and short stature.

8. Human chromosomal deficiency: the 4p--syndrome.

9. Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4.

10. Child with multiple anomalies and a group B(4-5) long arm deletion (Bq-).