Pages that link to "Q70076728"
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The following pages link to human chromosomes 4-5 (Q70076728):
Displaying 50 items.
- Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes (Q24564639) (← links)
- Linkage of the evolutionarily-related serum albumin and alpha-fetoprotein genes within q11-22 of human chromosome 4 (Q24675056) (← links)
- Possible Localization of Gc-System on Chromosome 4. Loss of Long Arm 4 Material Associated with Father-Child Incompatibility Within the Gc-System (Q28254093) (← links)
- Assignment of the gene for phosphoribosylpyrophosphate amidotransferase to the pter leads to q21 region of human chromosome 4 (Q28286974) (← links)
- Further data on the assignment of the phosphoglucomutase2 (PGM2) gene locus to chromosome 4 in man (Q30684067) (← links)
- Further data on the assignment of the phosphoglucomutase (PGM2) gene locus to chromosome 4 in man (Q30695146) (← links)
- A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)] (Q33586512) (← links)
- A family with an inherited translocation involving the no. 4/no. 21 chromosomes (Q33586695) (← links)
- Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison' (Q33586720) (← links)
- Reciprocal translocation, 4q-; 21p+, giving rise to Down's syndrome (Q33587090) (← links)
- Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation (Q33587393) (← links)
- Two reciprocal translocations associated with microcephaly and retardation (Q33587486) (← links)
- Prenatal recognition of 4p- syndrome (Q33587648) (← links)
- 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations (Q33587698) (← links)
- Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes (Q33588040) (← links)
- Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome (Q33588054) (← links)
- Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm (Q33588224) (← links)
- Translocation 4p-- syndrome: a general review (Q34162821) (← links)
- Regional localization of human phosphoglucomutase-2 locus on chromosome 4 (Q34236848) (← links)
- A polymorphic DNA marker genetically linked to Huntington's disease (Q34255139) (← links)
- Regional assignment of genes for phosphoglucomutase2 and peptidase S to 4pter leads to 4q21 in man (Q34292700) (← links)
- Human PGM2 (E.C. 2.7.5.1) mapped to 4pter leads to 4q25 (Q34292706) (← links)
- Mental retardation in a child with a long B-group chromosome (Q34632597) (← links)
- Deletion of short arm of no. 4 (4p-)--a detailed case report (Q34633639) (← links)
- Developmental abnormalities in a patient with karyotype 46,XX,bq+ (Q34633643) (← links)
- A deleted B chromosome in a mosaic mother and her cri du chat progeny (Q34633941) (← links)
- A family with balanced translocation, t(5p-;Gp+) (Q34634313) (← links)
- Congenital leukaemia with 46,XX,t(Bq+,Cq-) cells (Q34634558) (← links)
- A ring-4 chromosome in a patient with normal intelligence and short stature (Q34634602) (← links)
- Genetic analysis of the cell surface: association of human chromosome 5 with sensitivity to diphtheria toxin in mouse-human somatic cell hybrids (Q35081481) (← links)
- A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation (Q36062397) (← links)
- The Somatic Cell Genetics of Human Interferon: Assignment of Human Interferon Loci to Chromosomes 2 and 5 (Q37447316) (← links)
- Chromosomal assignment of the gene for the human beta 2-adrenergic receptor (Q37600854) (← links)
- Chromosome site for Epstein-Barr virus DNA in a Burkitt tumor cell line and in lymphocytes growth-transformed in vitro (Q37608005) (← links)
- Partial trisomy for the distal long arm of chromosome 5 (region q34 leads to qter). A new clinically recognizable syndrome (Q39208653) (← links)
- Translocation 46,XY,t(2;5) (q37;q14) and mental retardation. Clinical and cytogenetic study (Q39386847) (← links)
- Concerning the linkage relationships of the Gc and MNSs loci (Q39506085) (← links)
- Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatin (Q39523485) (← links)
- Genetic control of the interferon system (Q39620777) (← links)
- Ophthalmic Features of Chromosome Deletion 4p-(Wolf-Hirschhorn Syndrome) (Q39643339) (← links)
- Pathologic anatomy of the Wolf-Hirschhorn syndrome (partial monosomy 4p--) (Q39687102) (← links)
- Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21 (Q39802782) (← links)
- A t(5p-;21q+) translocation in a family with Down syndrome (Q39823972) (← links)
- The trisomy 4p syndrome: Case report and review (Q39876484) (← links)
- Bilateral neonatal Wilms' tumor with B-C chromosomal translocation (Q39917030) (← links)
- Autoradiography may be Unreliable for Identifying Human Chromosomes (Q39978627) (← links)
- Partial duplication of the long arm of chromosome 5: A case due to balanced paternal translocation and review of the literature (Q40015534) (← links)
- Simultaneous occurrence of ring "G" chromosome and group "B" pericentric inversion in the same individual: case report and review of the literature (Q40057168) (← links)
- Relationship of the characteristics of the chromosome set in human cell cultures to the production and antiviral action of interferon (Q40256162) (← links)
- Partial 4q trisomy. Apropos of 3 cases (Q40329943) (← links)