(Q40040214)

16 September 2017

1 reference

title

Dysmorphology (teratology) (English)

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80311-6

3 May 2023

author name string

D. W. Smith

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5332788

3 May 2023

language of work or name

English

0 references

publication date

1 December 1966

1 reference

full work available at URL

16 September 2017

https://api.elsevier.com/content/article/PII:S0022347666803116?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80311-6

https://api.elsevier.com/content/article/PII:S0022347666803116?httpAccept=text/plain

3 May 2023

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80311-6

The Journal of Pediatrics

3 May 2023

published in

1 reference

16 September 2017

volume

69

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16 September 2017

issue

6

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16 September 2017

page(s)

1150-1169

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TIMING OF HUMAN CONGENITAL MALFORMATIONS WITH A TIME-TABLE OF HUMAN DEVELOPMENT

16 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

THE EFFECT OF DRUGS UPON THE DEVELOPING FETUS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

RADIATION AND CONGENITAL MALFORMATIONS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

The inheritance of congenital pyloric stenosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Clefts of the lip and palate in twins; including a discordant pair whose monozygosity was confirmed by skin transplants

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Evidence of post-natal environmental influence in the aetiology of infantile pyloric stenosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

CONGENITAL ANOMALIES IN THE NEWBORN INFANT, INCLUDING MINOR VARIATIONS. A STUDY OF 4,412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES AND BUCCAL SMEAR FOR SEX CHROMATIN

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

CONGENITAL ANOMALIES ASSOCIATED WITH IDIOPATHIC MENTAL RETARDATION.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Finger-Prints, Palms and Chromosomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

The use of dermal configurations in the diagnosis of mongolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

DERMATOGLYPHIC ANOMALIES IN TURNER'S SYNDROME

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Unusual dermatoglyphic findings associated with rubella embryopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Inkless methods of finger, palm, and sole printing

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

7 January 2021

AUTOSOMAL ABNORMALITIES

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

THE SEX CHROMOSOME ANOMALIES.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Chromosome studies in eleven families with mongolism in more than one member

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Chromosomal translocations in patients with mongolism and in their normal relatives.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Chromosome studies in detection of parents with high risk of second child with Down's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

THE NONRANDOMNESS OF CHROMOSOMAL ABNORMALITIES. ASSOCIATION OF TRISOMY 18 AND DOWN'S SYNDROME

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

FAMILIAL MOSAICISM ATTRIBUTABLE TO A NEW GENE

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Incidence of infective hepatitis followed by Down's syndrome nine months later

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

LEUCOCYTE ENZYMES IN DOWN'S SYNDROME

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

NUCLEAR ABNORMALITIES OF THE NEUTROPHILS IN D1 (13-15)-TRISOMY SYNDROME

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

FOETAL HAEMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROME

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Anti-mongolism. Studies in an infant with a partial monosomy of the 21 chromosome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Hypospadias and other anomalies associated with partial deletion of short arms of chromosome 4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

CONGENITAL MALFORMATIONS IN NEWBORN INFANTS OF DIABETIC WOMEN. CORRELATION WITH MATERNAL DIABETIC VASCULAR COMPLICATIONS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Experimental diabetes in pregnant mice. Prevention of congenital malformations in offspring by insulin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

VIROLOGIC AND SEROLOGIC STUDIES ON HUMAN PRODUCTS OF CONCEPTION AFTER MATERNAL RUBELLA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

7 January 2021

Fetal rubella pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

The sensitive phase in thalidomide embryopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Teeth pigmented by tetracycline

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

TRANSPLACENTAL EFFECT OF TETRACYCLINES ON TEETH

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

THE OTOTOXICITY OF CHLOROQUINE PHOSPHATE.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

MATERNAL PHENYLKETONURIA. A CAUSE OF MENTAL RETARDATION IN CHILDREN WITHOUT THE METABOLIC DEFECT.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Phenylalanine: Transplacental centrations in Rhesus Monkeys

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Immunity in the foetus and the new-born

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

ATAXIA-TELANGIECTASIA. ITS ASSOCIATION WITH A DEFECTIVE THYMUS, IMMUNOLOGICAL-DEFICIENCY DISEASE, AND MALIGNANCY

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

Clinical and immunologic features of dysgammaglobulinemia type I. Report of a case diagnosed in the first year of life

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980311-6

The inheritance of common congenital malformations

7 January 2021

12

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80311-6

Familial nature of congenital heart diseases

3 May 2023

19

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80311-6

Chromosome studies of persons with mongolism (Down's syndrome) born to young mothers

3 May 2023

43

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80311-6

Partial 18 monosomy in the cyclops malformation

3 May 2023

65

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80311-6

Immunological deficiency diseases

3 May 2023

86

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80311-6

3 May 2023

Identifiers

1 reference

16 September 2017

1 reference