| P2093 | author name string | M G Wilson | |
| | E Siris | |
| | A J Ebbin | |
| | J W Towner | |
| | G S Coffin | |
| | P Brager | |
| P2860 | cites work | The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man | Q70344369 |
| | 4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat | Q70795706 |
| | Variation in Palmar Creases | Q71580527 |
| | Wolf-Hirschhorn syndrome | Q71838828 |
| | A rapid banding technique for human chromosomes | Q93712955 |
| | Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm | Q33588224 |
| | Translocation 4p-- syndrome: a general review | Q34162821 |
| | Deficiency on the short arms of a chromosome No. 4 | Q34241073 |
| | Deletion of short arms of chromosome 4?5 in a child with defects of midline fusion | Q34241369 |
| | Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4. | Q34633620 |
| | Inherited pericentric inversion of chromosome no. 4. | Q35232381 |
| | The Wolf-Hirschhorn syndrome. I. Genetics. | Q40362613 |
| | Ring of the chromosome 4. I - With 4p- phenotype | Q40656705 |
| | Ring of the chromosome 4. II. Without facial dysmorphism | Q40656711 |
| | Partial deletion of the short arm of chromosome 4. Apropos of 3 cases | Q40656755 |
| | Partial trisomy 10p of paternal origin. 2 new cases in 2 different families | Q40667767 |
| | The Wolf-Hirschhorn (4p-) syndrome. | Q41738439 |
| | Wolf's syndrome in twins -- translocation in the mother | Q41937204 |
| | Deletion of the short arm of chromosome 4 from a subject with Wolf's syndrome. Repository identification no. GM-72 | Q42801710 |
| | Ring chromosome 4 and Wolf syndrome | Q43879357 |
| | The Wolf-Hirschhorn syndrome. Deletion of the short arm of chromosome 4 | Q44787745 |
| | Systematic analysis of 95 reciprocal translocations of autosomes | Q44997574 |
| | Case report: partial trisomy 12p associated with 4p deletion due to paternal t(12p-;4p+) translocation | Q45056841 |
| | A syndrome of retarded development with characteristic appearance. | Q54260809 |
| | Partial trisomy 4p with translocation 4p-, 22p+ in the father. | Q54630111 |
| | The clinical and cytogenetic manifestations of four cases with partial deletion of the short arm of one of the chromosomes of group B | Q66863904 |
| | 4p- Phenotype in an Infant With t(4p-;19p or q + )mat Translocation | Q66918107 |
| | 4p monosomy with paternal t(13;14) (p11;p11) translocation | Q66931653 |
| | Trisomy 4p and Deletion 4p- in a Family having a Translocation, t(4p-; 12p+) | Q67252601 |
| | Partial deletion of 4p16 band in a ring chromosome and Wolf Syndrome | Q67404261 |
| | Proximal 4p-deletion: phenotype differs from classical 4p-syndrome | Q67538013 |
| | Wolf-Hirschhorn syndrome and balanced (4;10) translocation in the father | Q67653037 |
| | A 13-year-old girl with Wolf's syndrome and karyotype 46,XX,del(4)(pter integral p15::p12 integral qter),9qh+. Increased risk of structural chromosome abnormalities in the progeny of mothers with 9qh+ | Q67657697 |
| | [Trisomy 4p] | Q69144356 |
| | The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability | Q70030848 |
| P433 | issue | 4 | |
| P921 | main subject | Wolf-Hirschhorn syndrome | Q610075 |
| P304 | page(s) | 297-307 | |
| P577 | publication date | 1981-01-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)] | |
| P478 | volume | 59 | |