| Relation of parental age to rigidity in Huntington's disease |
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| Autosomal dominant pseudoxanthoma elasticum |
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| Textbook of Human Genetics |
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| Cystic fibrosis: current concepts. |
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| Effects of mitochondrial inhibition by chloramphenicol on the mitotic cycle of human cell cultures |
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| Presumptive Mosaic Partial Trisomy Associated with Congenital Anomalies and Mental Deficiency |
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| A family with two translocations and a polymorphism involving chromosome 14. |
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| Polysyndactyly and Marfan's syndrome |
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| A genetic register system (RAPID) |
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| Human Cytogenetics. Volume 1. General Cytogenetics. Volume 2. Clinical Cytogenetics. |
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| Comments upon the classification of infantile polycystic diseases of the liver and kidney, based upon three-dimensional reconstruction of the liver |
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| 21 Monosomy in a retarded female infant |
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| A case of partial trisomy 15 |
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| Turner Phenotype: Mosaic 45,X/47,XY,+18 |
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| Genetic Heterogeneity of Cebocephaly |
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| The Trismus-Pseudocampylodactyly Syndrome |
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| A Neurogenic Component in Muscular Dystrophy |
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| Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria. |
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| The significance of radiation-induced chromosome abnormalities in radiological protection |
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| Translocation, t(4q-;13q+), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation |
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| Letter: Seckel syndrome. |
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| Letter: Cellular metachromasia with toluidine blue O in cultured white cells of cystic fibrosis heterozygotes. |
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| Clinical Genetics, 2nd ed |
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| Pleiotropic effects of the gene for retinoblastoma |
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| Clinical variations of testicular intersexuality in a family |
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| Haemoglobin H disease and -thalassaemia: Clinical haematological and electrophoretic studies in a family from South Lebanon |
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| Familial translocation 15/22. A possible cause for abortions in female carriers |
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| Histidinaemia in a consanguineous marriage |
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| An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12 |
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| Down's syndrome associated with two Robertsonian translocations, 45,XX,-15,-21,+t(15q21q) and 46,XX,-21,+t(21q21q) |
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| Humanbiologie. (In German.) |
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| Racial variation in diabetes mellitus in Japanese and Caucasians living in Hawaii |
✓ |
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| Xerodermic idiocy in identical twins |
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| Chromosomal abnormality associated with congenital macroglossia and other abnormalities. |
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| Arthrogryposis Multiplex Congenita: Neurogenic Type with Autosomal Recessive Inheritance |
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| Evidence for mutation being the source of the abnormal gene for plasma cholinesterase |
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| Evidence for autosomal recessive inheritance in cerebral gigantism |
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| Extensive cytological damage caused by measles in African children |
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African children |
| Microphotometry of banded human chromosomes: High resolving power by direct scanning of the specimen compared with scanning on microphotographs |
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| Prenatal diagnosis: a problem in verification |
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| Familial thyroxine-binding globulin deficiency: search for linkage with Xg blood groups |
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| Another human chimaera |
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| Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness |
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| New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups |
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| Haemoglobin D Punjab (D Los Angeles) |
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| Prenatal evaluation in a case of familial Y chromosome long arm deletion (Yq--) |
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| Risk tables for genetic counselling in some common congenital malformations |
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| Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome |
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| SI Units |
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| Progeria in twins |
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| Karyotype 45,XX,-21/46,XX,21q- in an infant with symptoms of G-deletion syndrome I |
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| The trisomy 8 syndrome: two additional mosaic cases |
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| Prenatal detection of D trisomy |
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| Turner's syndrome and 46,X,i(Yq) karyotype |
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| Lionel Sharples Penrose (1898-1972). |
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| Haemoglobin F Malaysia: 2 2 1 (NA1) Glycine->Cysteine; 136 Glycine |
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| Craniorachischisis in a Partially Trisomic 11 Fetus in a family with Reproductive Failure and a Reciprocal Translocation, t(6p+;11q-) |
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| Double Autosomal Trisomy and Mosaicism for Chromosomes No. 8 and No. 21 |
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| Muscle ribosomal protein synthesis in normal pregnancy: implication for carrier detection in Duchenne muscular dystrophy |
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| Fabry's disease: specific inclusions found on electron microscopy of fibroblast cultures |
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| Absence of the 9q+chromosome in Ph1 negative chronic myelogenous leukaemia |
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| Frequency of deletion of short arm satellites in acrocentric chromosomes |
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| Observations on human amniotic fluid cell strains in serial culture |
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| Deletion of the long arms of the Y chromosome with normal male development and intelligence |
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| A 48,XXXX female |
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| Effects of cystic fibrosis sera on Proteus vulgaris motility |
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| Multiple congenital defects associated with trisomy for the short arm of chromosome 4 |
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| The Prenatal Diagnosis of Hereditary Disorders |
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| Absence of the -thalassaemia syndromes in Egyptian Arabs |
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| Haptoglobins in chronic lymphatic leukaemia |
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| Three generations and seven family members with a t(21q22q) chromosome. |
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| Correction |
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| A Kindred with Familial Cold Urticaria: Linkage Analysis |
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| An Analysis of the Break Points of Structural Rearrangements in Man |
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| Immunoglobulins. |
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| A Case of Meningomyelocele in a Kindred with Multiple Cases of Spondylolisthesis and Spina Bifida Occulta |
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| Sanfilippo A disease in the fetus |
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| A sporadic case of apparent Crouzon's syndrome with extracraniofacial manifestations |
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| Inherited partial duplication of chromosome No. 15 |
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| A 21/21 tandem translocation with satellites on both long and short arms |
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| Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother |
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| Human Chromosomes |
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| -Thalassaemia in two Turkish families |
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| Chromocentres in polymorphs as interphase markers for chromosomes having increased constitutive heterochromatin |
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| X-linked mental retardation |
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| Congenital limb anomalies: frequency and aetiological factors: Data from the Edinburgh Register of the Newborn (1964-68) |
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| Mitochondrial inclusions in fibroblast culture from a patient with -methylcrotonylglycinuria |
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| 48,XXX, +18 double trisomy |
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| The tricho-rhino-phalangeal syndrome |
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| Familial mental retardation in a family with an inherited chromosome rearrangement |
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