-
[PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].
Pathol Biol. 1964 May;12:579-82
PMID: 14180960
-
PHENOTYPIC SHIFTS IN TRISOMY.
Am J Hum Genet. 1965 Mar;17:111-24
PMID: 14262129
-
The leucocyte alkaline phosphatase in mongolism.
Lancet. 1962 Sep 8;2(7254):486-7
PMID: 13922647
-
[Studies on the activity of galactokinase in the blood of normal persons and of patients with GDo trisomy].
Humangenetik. 1965;1(3):279-88
PMID: 4223835
-
THE "CAT CRY" SYNDROME.
Am J Dis Child. 1964 Nov;108:538-42
PMID: 14209690
-
[Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].
Ann Genet. 1966 Sep;9(3):113-22
PMID: 5298289
-
FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.
Am J Hum Genet. 1965 Sep;17:410-9
PMID: 14334740
-
[FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION].
Ann Genet. 1964;7:76-83
PMID: 14249002
-
"CRI DU CHAT" SYNDROME. A NEW CLINICAL AND CYTOGENETIC ENTITY.
Lancet. 1965 Jan 2;1(7375):23-5
PMID: 14246676
-
GALACTOSAEMIA LOCUS AND THE DOWN'S SYNDROME CHROMOSOME.
Lancet. 1963 Oct 5;2(7310):700-3
PMID: 14057154
-
Alkaline-phosphatase activity of polymorphs in mongolism.
Lancet. 1962 Dec 22;2(7269):1302-5
PMID: 14032857
-
[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].
C R Hebd Seances Acad Sci. 1964 Nov 30;259:4187-90
PMID: 14260664
-
ENHANCEMENT OF ERYTHROCYTE-GALACTOKINASE ACTIVITY IN LANGDON-DOWN TRISOMY.
Lancet. 1965 Mar 6;1(7384):553
PMID: 14251534
-
Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.
Chromosoma. 1961;12:573-84
PMID: 14484286
-
[Study of somatic chromosomes from 9 mongoloid children].
C R Hebd Seances Acad Sci. 1959 Mar 16;248(11):1721-2
PMID: 13639368
-
A new trisomic syndrome.
Lancet. 1960 Apr 9;1(7128):787-90
PMID: 13819419
-
CHROMOSOME STUDIES DURING EARLY AND TERMINAL CHRONIC MYELOID LEUKAEMIA.
Br Med J. 1964 Apr 18;1(5389):1010-4
PMID: 14113474
-
AUTOSOMALLY DETERMINED POLYMORPHISM OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN PEROMYSCUS.
Science. 1965 May 21;148(3673):1099-100
PMID: 14289612
-
[5-21-22 translocation and the crying cat syndrome].
Ann Genet. 1965;8(1):31-8
PMID: 5294631
-
The leucocyte count in children with mongolism.
J Ment Sci. 1958 Apr;104(435):457-60
PMID: 13564152
-
A possible specific chromosome abnormality in human chronic myeloid leukaemia.
Nature. 1960 Dec 31;188:1165-6
PMID: 13685929
-
The chromosomes of man.
Nature. 1956 Nov 10;178(4541):1020-3
PMID: 13378517
-
MEASUREMENTS OF LIKENESS IN RELATIVES OF TRISOMICS.
Ann Hum Genet. 1963 Nov;27:183-7
PMID: 14081489
-
MULTIPLE FORMS OF ENZYMES: TISSUE, ONTOGENETIC, AND SPECIES SPECIFIC PATTERNS.
Proc Natl Acad Sci U S A. 1959 May;45(5):753-63
PMID: 16590440
-
[Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state].
Ann Genet. 1966;9(1):32-8
PMID: 5295700
-
LE CRI DU CHAT (CRYING CAT) SYNDROME.
Am J Dis Child. 1964 Nov;108:533-7
PMID: 14209689
-
[Deletion of the short arms of chromosome No. 18].
Humangenetik. 1966;2(2):178-85
PMID: 5915640
-
Blood-group gene localization through a study of mongolism.
Ann Hum Genet. 1966 Jul;30(1):49-67
PMID: 4225588
-
SPECIFICITY OF THE PHILADELPHIA CHROMOSOME; CYTOGENIC STUDIES IN CASES OF CHRONIC MYELOCYTIC LEUKEMIA AND MYELOID METAPLASIA.
Ann Intern Med. 1964 Oct;61:609-24
PMID: 14217124
-
Completeness of catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes.
Am J Med Genet. 1992 Jun 1;43(3):606-8
PMID: 1605257
-
Genetics of fourteen marker systems: associations and linkage relations.
Acta Genet Stat Med. 1966;16(1):1-58
PMID: 4955839
-
[FACTOR MAP OUTLINE OF THE X CHROMOSOME].
Ann Genet. 1964;7:101-5
PMID: 14248997
-
ABO FREQUENCIES IN MONGOLS.
Ann Hum Genet. 1964 Jun;27:405-12
PMID: 14175204
-
[Deletion of the short arm of chromosome 18].
Ann Genet. 1966;9(1):19-26
PMID: 5295699
-
Electrophoretic variation in enzymes.
Science. 1965 Aug 27;149(3687):936-43
PMID: 5318249
-
DELETION OF THE SHORT ARM OF CHROMOSOME 18.
Cytogenetics. 1964;3:201-6
PMID: 14227324
-
STUDIES OF THE PHILADELPHIA CHROMOSOME IN PATIENTS WITH CHRONIC MYELOGENOUS LEUKEMIA.
Ann N Y Acad Sci. 1964 Feb 28;113:1073-80
PMID: 14120508
-
[On a case of partial deletion of the short arm of chromosome 18, resulting in a familial 18c-17 translocation].
Ann Genet. 1966;9(1):27-31
PMID: 5295911
-
The Duffy blood groups of New York negroes: the phenotype Fy (a-b-).
Br J Haematol. 1955 Oct;1(4):370-4
PMID: 13269673
-
Multiple molecular forms of leucine aminopeptidase in man.
Acta Genet Stat Med. 1966;16(3):223-30
PMID: 5953709
-
ABO BLOOD GROUPS OF MONGOLS.
Can Med Assoc J. 1963 Oct 26;89:906
PMID: 14069621
-
HUMAN RED-CELL PHOSPHOGLUCONATE DEHYDROGENASES.
Nature. 1963 Nov 30;200:890-1
PMID: 14096069
-
Bivalent alleles.
Am J Hum Genet. 1966 May;18(3):233-42
PMID: 5944417
-
PARTIAL DELETION OF SHORT ARMS OF CHROMOSOME NO. 5. REPORT OF A CASE IN A FRATERNAL TWIN.
Am J Dis Child. 1965 Jan;109:85-9
PMID: 14218865
-
ABO frequencies in mongolism.
Ann Hum Genet. 1966 Jul;30(1):43-8
PMID: 4225587
-
[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
C R Hebd Seances Acad Sci. 1963 Nov 18;257:3098-102
PMID: 14095841
-
[PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE].
Sem Hop. 1964 Apr 14;40:1069-79
PMID: 14144301
-
Hexose-6-phosphate dehydrogenase found in human liver.
Science. 1966 Aug 26;153(3739):1015-6
PMID: 5917551
-
LEUCOCYTE ALKALINE PHOSPHATASE IN KLINEFELTER'S SYNDROME.
J Med Genet. 1965 Jun;2(2):112-5
PMID: 14295652
-
Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults.
Biochem J. 1955 Dec;61(4):629-41
PMID: 13276348
-
Further studies on the genetics of placental alkaline phosphatase.
Ann Hum Genet. 1967 Jan;30(3):219-32
PMID: 6067798
-
Catalase Hybrid Enzymes in Maize.
Science. 1964 Nov 27;146(3648):1174-5
PMID: 17832245
-
[Chromosomal studies in chronic myeloic leukemia].
Klin Wochenschr. 1966 Jan 1;44(1):12-9
PMID: 5234187
-
[To the formal genetics of the Duffy system. Investigation of 247 families].
Humangenetik. 1967;4(1):59-61
PMID: 6081913
-
ACID-PHOSPHATASE ACTIVITY IN PARTIAL TRANSLOCATION-TRISOMY.
Lancet. 1965 Apr 3;1(7388):768
PMID: 14255264
-
Anti-mongolism. Studies in an infant with a partial monosomy of the 21 chromosome.
Lancet. 1966 Feb 19;1(7434):394-7
PMID: 4159779
-
STUDIES ON GALACTOSE OXIDATION IN DOWN'S SYNDROME.
N Engl J Med. 1964 May 21;270:1085-8
PMID: 14121488
-
[Deficiency on the short arms of a chromosome No. 4].
Humangenetik. 1965;1(5):397-413
PMID: 5868696
-
Multiple congenital anomaly caused by an extra autosome.
Lancet. 1960 Apr 9;1(7128):790-3
PMID: 14430807
-
GENETIC STUDIES ON MUTANT ENZYMES IN MAIZE: SYNTHESIS OF HYBRID ENZYMES BY HETEROZYGOTES.
Proc Natl Acad Sci U S A. 1960 Sep;46(9):1210-5
PMID: 16590735
-
[Deletion of the short arm of a 13-15 chromosome, hypertelorism and Hp0 haptoglobin phenotype in the same family].
Ann Genet. 1966 Jun;9(2):80-5
PMID: 5296303
-
[Clinical and genetic studies of a patient with crying cat syndrome].
Dtsch Med Wochenschr. 1965 Nov 5;90(45):2008-13
PMID: 5833954
-
UNUSUAL INHERITANCE OF ABO GROUP IN A FAMILY WITH WEAK B ANTIGENS.
Vox Sang. 1964 May-Jun;9:268-77
PMID: 14170898
-
A search for autosomal linkage in a trisomic population: blood group frequencies in Mongols.
Am J Hum Genet. 1962 Dec;14:317-34
PMID: 13976965
-
STUDIES OF LEUKOCYTE ALKALINE PHOSPHATASE IN MONGOLISM: A POSSIBLE CHROMOSOME MARKER.
Blood. 1963 Aug;22:165-77
PMID: 14045301
-
Lactate dehydrogenase variant from human blood: evidence for molecular subunits.
Science. 1963 Aug 16;141(3581):642-3
PMID: 14014718
-
Mnifold chromosome abnormalities in leukaemia.
Lancet. 1962 May 26;1(7239):1098-100
PMID: 14004414
-
CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.
Ann Hum Genet. 1963 Nov;27:171-4
PMID: 14081487
-
[THE CRYING CAT SYNDROME: A FURTHER CASE].
Ann Genet. 1964;7:13-6
PMID: 14242102
-
PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
Am J Hum Genet. 1964 Sep;16:364-74
PMID: 14207551
-
PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER).
Arch Dis Child. 1965 Feb;40:82-5
PMID: 14259280
-
Genotypic distribution among human autosomal aneuploids: a theoretical consideration.
Acta Genet Stat Med. 1963;13:67-76
PMID: 13991052
-
[Exclusion of certain autosomal localizations of blood and serum group genes].
Ann Genet. 1966;9(1):9-11
PMID: 5295703
-
"Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case.
Maandschr Kindergeneeskd. 1965 Aug;33(8):286-98
PMID: 5848077
-
[Studies on "branched chain oxoacid aciduria" (maple syrup diseases)].
Med Klin. 1966 Dec 30;61(52):2063-7
PMID: 4385693